Canonical Allele Identifier: CA357516831

Gene: H2AZ1

Linked Data

• MyVariant Identifiers: chr4:g.100870833C>T (hg19) ; chr4:g.99949676C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949676C>T , CM000666.2:g.99949676C>T	GRCh38
NC_000004.11:g.100870833C>T , CM000666.1:g.100870833C>T	GRCh37
NC_000004.10:g.101089856C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.68G>A MANE Select	ENSP00000296417.5:p.Arg23Lys
ENST00000651623.1:c.68G>A	ENSP00000498935.1:p.Arg23Lys
ENST00000296417.5:c.68G>A	ENSP00000296417.5:p.Arg23Lys
ENST00000511203.1:n.624G>A
ENST00000511319.5:n.593G>A
ENST00000511348.1:n.253G>A
ENST00000527366.1:n.152G>A
ENST00000529158.5:n.117G>A
NM_002106.3:c.68G>A	NP_002097.1:p.Arg23Lys
NM_002106.4:c.68G>A MANE Select	NP_002097.1:p.Arg23Lys