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H2AZ2P1 H2AZ2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 654500, updated on 23-Nov-2021

Summary

Official Symbol
H2AZ2P1provided by HGNC
Official Full Name
H2AZ2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:31026
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
H2AFVP; H2AFVP1; HsT19970
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Genomic context

See H2AZ2P1 in Genome Data Viewer
Location:
15q26.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (92733616..92734276, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (93276846..93277506, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene family with sequence similarity 174 member B Neighboring gene high mobility group nucleosome binding domain 1 pseudogene 38 Neighboring gene ribosomal protein L31 pseudogene 6 Neighboring gene ferritin light chain pseudogene Neighboring gene uncharacterized LOC101926994

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • H2A histone family member V pseudogene 1
  • H2A histone family, member V pseudogene

NCBI Reference Sequences (RefSeq)

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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_009543.3 

    Range
    101..761
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    92733616..92734276 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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