Canonical Allele Identifier: CA357517011
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870863G>C (hg19) chr4:g.99949706G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949706G>C , CM000666.2:g.99949706G>C GRCh38
NC_000004.11:g.100870863G>C , CM000666.1:g.100870863G>C GRCh37
NC_000004.10:g.101089886G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.38C>G MANE Select ENSP00000296417.5:p.Ala13Gly
ENST00000651623.1:c.38C>G ENSP00000498935.1:p.Ala13Gly
ENST00000296417.5:c.38C>G ENSP00000296417.5:p.Ala13Gly
ENST00000511203.1:n.594C>G
ENST00000511319.5:n.563C>G
ENST00000511348.1:n.223C>G
ENST00000527366.1:n.122C>G
ENST00000529158.5:n.87C>G
NM_002106.3:c.38C>G NP_002097.1:p.Ala13Gly
NM_002106.4:c.38C>G MANE Select NP_002097.1:p.Ala13Gly
Search 100 bp 5'
Search 100 bp 3'