Canonical Allele Identifier: CA3693022
Gene: HLA-A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1059418

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29942785A>C , CM000668.2:g.29942785A>C GRCh38
NC_000006.10:g.30018541A>C NCBI36
NC_000006.11:g.29910562A>C , CM000668.1:g.29910562A>C GRCh37
NG_029217.2:g.5320A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376802.2:c.102A>C ENSP00000365998.2:p.Thr34=
ENST00000376806.9:c.102A>C ENSP00000366002.5:p.Thr34=
ENST00000376809.9:c.102A>C ENSP00000366005.5:p.Thr34=
ENST00000396634.5:c.102A>C ENSP00000379873.1:p.Thr34=
ENST00000429656.1:n.283T>G
ENST00000461903.1:n.102A>C
ENST00000479320.5:n.102A>C
ENST00000495183.5:n.104A>C
ENST00000496081.5:n.108A>C
NM_002116.7:c.102A>C NP_002107.3:p.Thr34=