Canonical Allele Identifier: CA440341295

Gene: H2AZ1

Linked Data

• dbSNP Id: rs11554382
• gnomAD v4: 4-99949696-C-T
• MyVariant Identifiers: chr4:g.100870853C>T (hg19) ; chr4:g.99949696C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949696C>T , CM000666.2:g.99949696C>T	GRCh38
NC_000004.11:g.100870853C>T , CM000666.1:g.100870853C>T	GRCh37
NC_000004.10:g.101089876C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296417.6:c.48G>A MANE Select	ENSP00000296417.5:p.Lys16=
ENST00000651623.1:c.48G>A	ENSP00000498935.1:p.Lys16=
ENST00000296417.5:c.48G>A	ENSP00000296417.5:p.Lys16=
ENST00000511203.1:n.604G>A
ENST00000511319.5:n.573G>A
ENST00000511348.1:n.233G>A
ENST00000527366.1:n.132G>A
ENST00000529158.5:n.97G>A
NM_002106.3:c.48G>A	NP_002097.1:p.Lys16=
NM_002106.4:c.48G>A MANE Select	NP_002097.1:p.Lys16=