Canonical Allele Identifier: CA440341307
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870874G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949717G>A , CM000666.2:g.99949717G>A GRCh38
NC_000004.11:g.100870874G>A , CM000666.1:g.100870874G>A GRCh37
NC_000004.10:g.101089897G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.27C>T MANE Select ENSP00000296417.5:p.Asp9=
ENST00000651623.1:c.27C>T ENSP00000498935.1:p.Asp9=
ENST00000296417.5:c.27C>T ENSP00000296417.5:p.Asp9=
ENST00000511203.1:n.583C>T
ENST00000511319.5:n.552C>T
ENST00000511348.1:n.212C>T
ENST00000527366.1:n.111C>T
ENST00000529158.5:n.76C>T
NM_002106.3:c.27C>T NP_002097.1:p.Asp9=
NM_002106.4:c.27C>T MANE Select NP_002097.1:p.Asp9=