Canonical Allele Identifier: CA357516976

Gene: H2AZ1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.44C>A MANE Select	ENSP00000296417.5:p.Thr15Lys
ENST00000651623.1:c.44C>A	ENSP00000498935.1:p.Thr15Lys
ENST00000296417.5:c.44C>A	ENSP00000296417.5:p.Thr15Lys
ENST00000511203.1:n.600C>A
ENST00000511319.5:n.569C>A
ENST00000511348.1:n.229C>A
ENST00000527366.1:n.128C>A
ENST00000529158.5:n.93C>A
NM_002106.3:c.44C>A	NP_002097.1:p.Thr15Lys
NM_002106.4:c.44C>A MANE Select	NP_002097.1:p.Thr15Lys