Canonical Allele Identifier: CA3710564
Gene: HLA-C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050317

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270358G>A , CM000668.2:g.31270358G>A GRCh38
NC_000006.10:g.31346114G>A NCBI36
NC_000006.11:g.31238135G>A , CM000668.1:g.31238135G>A GRCh37
NG_029422.2:g.6774C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.9:c.747C>T ENSP00000365402.5:p.Thr249=
ENST00000376237.8:c.*334C>T ENSP00000365412.4:p.=
ENST00000383329.7:c.747C>T ENSP00000372819.3:p.Thr249=
ENST00000415537.1:n.665-27C>T
ENST00000470363.5:n.65C>T
ENST00000487245.5:n.1106C>T
ENST00000495835.1:n.936C>T
NM_002117.5:c.747C>T NP_002108.4:p.Thr249=