Canonical Allele Identifier: CA136023542
Gene: HLA-A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs199474537

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943407C>T , CM000668.2:g.29943407C>T GRCh38
NC_000006.11:g.29911184C>T , CM000668.1:g.29911184C>T GRCh37
NC_000006.10:g.30019163C>T NCBI36
NG_029217.2:g.5942C>T

Transcript Alleles

HGVS Amino-acid change
NM_002116.7:c.483C>T VV NP_002107.3:p.Asp161=
NM_002116.8:c.483C>T VV MANE Preferred NP_002107.3:p.Asp161=
ENST00000376802.2:c.483C>T ENSP00000365998.2:p.Asp161=
ENST00000376806.9:c.483C>T ENSP00000366002.5:p.Asp161=
ENST00000376809.9:c.483C>T ENSP00000366005.5:p.Asp161=
ENST00000396634.5:c.483C>T ENSP00000379873.1:p.Asp161=
ENST00000461903.1:n.724C>T
ENST00000479320.5:n.724C>T
ENST00000495183.5:n.726C>T
ENST00000496081.5:n.300C>T