Canonical Allele Identifier: CA440341300

Gene: H2AZ1

Linked Data

• MyVariant Identifiers: chr4:g.100870862G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949705G>T , CM000666.2:g.99949705G>T	GRCh38
NC_000004.11:g.100870862G>T , CM000666.1:g.100870862G>T	GRCh37
NC_000004.10:g.101089885G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.39C>A MANE Select	ENSP00000296417.5:p.Ala13=
ENST00000651623.1:c.39C>A	ENSP00000498935.1:p.Ala13=
ENST00000296417.5:c.39C>A	ENSP00000296417.5:p.Ala13=
ENST00000511203.1:n.595C>A
ENST00000511319.5:n.564C>A
ENST00000511348.1:n.224C>A
ENST00000527366.1:n.123C>A
ENST00000529158.5:n.88C>A
NM_002106.3:c.39C>A	NP_002097.1:p.Ala13=
NM_002106.4:c.39C>A MANE Select	NP_002097.1:p.Ala13=