Canonical Allele Identifier: CA102666209

Gene: H2AZ1

Linked Data

• dbSNP Id: rs11554387
• MyVariant Identifiers: chr4:g.100870873A>G (hg19) ; chr4:g.99949716A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949716A>G , CM000666.2:g.99949716A>G	GRCh38
NC_000004.11:g.100870873A>G , CM000666.1:g.100870873A>G	GRCh37
NC_000004.10:g.101089896A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.28T>C MANE Select	ENSP00000296417.5:p.Ser10Pro
ENST00000651623.1:c.28T>C	ENSP00000498935.1:p.Ser10Pro
ENST00000296417.5:c.28T>C	ENSP00000296417.5:p.Ser10Pro
ENST00000511203.1:n.584T>C
ENST00000511319.5:n.553T>C
ENST00000511348.1:n.213T>C
ENST00000527366.1:n.112T>C
ENST00000529158.5:n.77T>C
NM_002106.3:c.28T>C	NP_002097.1:p.Ser10Pro
NM_002106.4:c.28T>C MANE Select	NP_002097.1:p.Ser10Pro