Canonical Allele Identifier: CA3693419
Gene: HLA-A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1059542

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943479T>A , CM000668.2:g.29943479T>A GRCh38
NC_000006.10:g.30019235T>A NCBI36
NC_000006.11:g.29911256T>A , CM000668.1:g.29911256T>A GRCh37
NG_029217.2:g.6014T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376802.2:c.555T>A ENSP00000365998.2:p.Asp185Glu
ENST00000376806.9:c.555T>A ENSP00000366002.5:p.Asp185Glu
ENST00000376809.9:c.555T>A ENSP00000366005.5:p.Asp185Glu
ENST00000396634.5:c.555T>A ENSP00000379873.1:p.Asp185Glu
ENST00000461903.1:n.796T>A
ENST00000479320.5:n.796T>A
ENST00000495183.5:n.798T>A
ENST00000496081.5:n.372T>A
NM_002116.7:c.555T>A NP_002107.3:p.Asp185Glu