Canonical Allele Identifier: CA440341311
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1288489458
gnomAD v2: 4-100870880-T-C
gnomAD v4: 4-99949723-T-C
MyVariant Identifiers: chr4:g.100870880T>C (hg19) chr4:g.99949723T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949723T>C , CM000666.2:g.99949723T>C GRCh38
NC_000004.11:g.100870880T>C , CM000666.1:g.100870880T>C GRCh37
NC_000004.10:g.101089903T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.21A>G MANE Select ENSP00000296417.5:p.Gly7=
ENST00000651623.1:c.21A>G ENSP00000498935.1:p.Gly7=
ENST00000296417.5:c.21A>G ENSP00000296417.5:p.Gly7=
ENST00000511203.1:n.577A>G
ENST00000511319.5:n.546A>G
ENST00000511348.1:n.206A>G
ENST00000527366.1:n.105A>G
ENST00000529158.5:n.70A>G
NM_002106.3:c.21A>G NP_002097.1:p.Gly7=
NM_002106.4:c.21A>G MANE Select NP_002097.1:p.Gly7=
Search 100 bp 5'
Search 100 bp 3'