Canonical Allele Identifier: CA357516961

Gene: H2AZ1

Linked Data

• MyVariant Identifiers: chr4:g.100870854T>A (hg19) ; chr4:g.99949697T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949697T>A , CM000666.2:g.99949697T>A	GRCh38
NC_000004.11:g.100870854T>A , CM000666.1:g.100870854T>A	GRCh37
NC_000004.10:g.101089877T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.47A>T MANE Select	ENSP00000296417.5:p.Lys16Met
ENST00000651623.1:c.47A>T	ENSP00000498935.1:p.Lys16Met
ENST00000296417.5:c.47A>T	ENSP00000296417.5:p.Lys16Met
ENST00000511203.1:n.603A>T
ENST00000511319.5:n.572A>T
ENST00000511348.1:n.232A>T
ENST00000527366.1:n.131A>T
ENST00000529158.5:n.96A>T
NM_002106.3:c.47A>T	NP_002097.1:p.Lys16Met
NM_002106.4:c.47A>T MANE Select	NP_002097.1:p.Lys16Met