U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

IGHVII-20-1 immunoglobulin heavy variable (II)-20-1 (pseudogene) [ Homo sapiens (human) ]

Gene ID: 28375, updated on 10-Oct-2023

Summary

Official Symbol
IGHVII-20-1provided by HGNC
Official Full Name
immunoglobulin heavy variable (II)-20-1 (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:5672
See related
IMGT/GENE-DB:IGHV(II)-20-1; AllianceGenome:HGNC:5672
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
4-20.1P; IGHVII201
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See IGHVII-20-1 in Genome Data Viewer
Location:
14q32.33
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (106212786..106212824, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (100484330..100484368, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (106669426..106669464, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene immunoglobulin heavy locus Neighboring gene uncharacterized LOC105370700 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:106657005-106658204 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr14:106662526-106663725 Neighboring gene ReSE screen-validated silencer GRCh37_chr14:106714469-106714636 Neighboring gene immunoglobulin heavy variable 3-19 (pseudogene) Neighboring gene immunoglobulin heavy variable 3-20 Neighboring gene immunoglobulin heavy variable 3-21 Neighboring gene immunoglobulin heavy variable 3-22 (pseudogene)

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_001019.6 

    Range
    667521..667559
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    106212786..106212824 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187600.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    680555..680593 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    100484330..100484368 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)