Canonical Allele Identifier: CA440341317
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870889A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949732A>C , CM000666.2:g.99949732A>C GRCh38
NC_000004.11:g.100870889A>C , CM000666.1:g.100870889A>C GRCh37
NC_000004.10:g.101089912A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.12T>G MANE Select ENSP00000296417.5:p.Gly4=
ENST00000651623.1:c.12T>G ENSP00000498935.1:p.Gly4=
ENST00000296417.5:c.12T>G ENSP00000296417.5:p.Gly4=
ENST00000511203.1:n.568T>G
ENST00000511319.5:n.537T>G
ENST00000511348.1:n.197T>G
ENST00000527366.1:n.96T>G
ENST00000529158.5:n.61T>G
NM_002106.3:c.12T>G NP_002097.1:p.Gly4=
NM_002106.4:c.12T>G MANE Select NP_002097.1:p.Gly4=