Canonical Allele Identifier: CA357517119

Gene: H2AZ1

Linked Data

• MyVariant Identifiers: chr4:g.100870888T>A (hg19) ; chr4:g.99949731T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949731T>A , CM000666.2:g.99949731T>A	GRCh38
NC_000004.11:g.100870888T>A , CM000666.1:g.100870888T>A	GRCh37
NC_000004.10:g.101089911T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.13A>T MANE Select	ENSP00000296417.5:p.Lys5Ter
ENST00000651623.1:c.13A>T	ENSP00000498935.1:p.Lys5Ter
ENST00000296417.5:c.13A>T	ENSP00000296417.5:p.Lys5Ter
ENST00000511203.1:n.569A>T
ENST00000511319.5:n.538A>T
ENST00000511348.1:n.198A>T
ENST00000527366.1:n.97A>T
ENST00000529158.5:n.62A>T
NM_002106.3:c.13A>T	NP_002097.1:p.Lys5Ter
NM_002106.4:c.13A>T MANE Select	NP_002097.1:p.Lys5Ter