Canonical Allele Identifier: CA440341306
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870871G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949714G>T , CM000666.2:g.99949714G>T GRCh38
NC_000004.11:g.100870871G>T , CM000666.1:g.100870871G>T GRCh37
NC_000004.10:g.101089894G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.30C>A MANE Select ENSP00000296417.5:p.Ser10=
ENST00000651623.1:c.30C>A ENSP00000498935.1:p.Ser10=
ENST00000296417.5:c.30C>A ENSP00000296417.5:p.Ser10=
ENST00000511203.1:n.586C>A
ENST00000511319.5:n.555C>A
ENST00000511348.1:n.215C>A
ENST00000527366.1:n.114C>A
ENST00000529158.5:n.79C>A
NM_002106.3:c.30C>A NP_002097.1:p.Ser10=
NM_002106.4:c.30C>A MANE Select NP_002097.1:p.Ser10=