Canonical Allele Identifier: CA3693197
Gene: HLA-A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs199474463

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943005T>C , CM000668.2:g.29943005T>C GRCh38
NC_000006.11:g.29910782T>C , CM000668.1:g.29910782T>C GRCh37
NC_000006.10:g.30018761T>C NCBI36
NG_029217.2:g.5540T>C

Transcript Alleles

HGVS Amino-acid change
NM_002116.7:c.322T>C VV NP_002107.3:p.Tyr108His
NM_002116.8:c.322T>C VV MANE Preferred NP_002107.3:p.Tyr108His
ENST00000376802.2:c.322T>C ENSP00000365998.2:p.Tyr108His
ENST00000376806.9:c.322T>C ENSP00000366002.5:p.Tyr108His
ENST00000376809.9:c.322T>C ENSP00000366005.5:p.Tyr108His
ENST00000396634.5:c.322T>C ENSP00000379873.1:p.Tyr108His
ENST00000429656.1:n.63A>G
ENST00000461903.1:n.322T>C
ENST00000479320.5:n.322T>C
ENST00000495183.5:n.324T>C
ENST00000496081.5:n.177+151T>C