Canonical Allele Identifier: CA357516972

Gene: H2AZ1

Linked Data

• MyVariant Identifiers: chr4:g.100870857G>A (hg19) ; chr4:g.99949700G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949700G>A , CM000666.2:g.99949700G>A	GRCh38
NC_000004.11:g.100870857G>A , CM000666.1:g.100870857G>A	GRCh37
NC_000004.10:g.101089880G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.44C>T MANE Select	ENSP00000296417.5:p.Thr15Ile
ENST00000651623.1:c.44C>T	ENSP00000498935.1:p.Thr15Ile
ENST00000296417.5:c.44C>T	ENSP00000296417.5:p.Thr15Ile
ENST00000511203.1:n.600C>T
ENST00000511319.5:n.569C>T
ENST00000511348.1:n.229C>T
ENST00000527366.1:n.128C>T
ENST00000529158.5:n.93C>T
NM_002106.3:c.44C>T	NP_002097.1:p.Thr15Ile
NM_002106.4:c.44C>T MANE Select	NP_002097.1:p.Thr15Ile