Canonical Allele Identifier: CA440341296
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870856T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949699T>A , CM000666.2:g.99949699T>A GRCh38
NC_000004.11:g.100870856T>A , CM000666.1:g.100870856T>A GRCh37
NC_000004.10:g.101089879T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296417.6:c.45A>T MANE Select ENSP00000296417.5:p.Thr15=
ENST00000651623.1:c.45A>T ENSP00000498935.1:p.Thr15=
ENST00000296417.5:c.45A>T ENSP00000296417.5:p.Thr15=
ENST00000511203.1:n.601A>T
ENST00000511319.5:n.570A>T
ENST00000511348.1:n.230A>T
ENST00000527366.1:n.129A>T
ENST00000529158.5:n.94A>T
NM_002106.3:c.45A>T NP_002097.1:p.Thr15=
NM_002106.4:c.45A>T MANE Select NP_002097.1:p.Thr15=