Canonical Allele Identifier: CA136019740
Gene: HLA-A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs199474412

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29942914G>A , CM000668.2:g.29942914G>A GRCh38
NC_000006.10:g.30018670G>A NCBI36
NC_000006.11:g.29910691G>A , CM000668.1:g.29910691G>A GRCh37
NG_029217.2:g.5449G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376802.2:c.231G>A ENSP00000365998.2:p.Glu77=
ENST00000376806.9:c.231G>A ENSP00000366002.5:p.Glu77=
ENST00000376809.9:c.231G>A ENSP00000366005.5:p.Glu77=
ENST00000396634.5:c.231G>A ENSP00000379873.1:p.Glu77=
ENST00000429656.1:n.154C>T
ENST00000461903.1:n.231G>A
ENST00000479320.5:n.231G>A
ENST00000495183.5:n.233G>A
ENST00000496081.5:n.177+60G>A
NM_002116.7:c.231G>A NP_002107.3:p.Glu77=