Canonical Allele Identifier: CA1619077165
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268922G= , CM000668.2:g.31268922G= GRCh38
NC_000006.11:g.31236699G= , CM000668.1:g.31236699G= GRCh37
NC_000006.10:g.31344678G= NCBI36
NG_029422.2:g.8210C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*247C= MANE Select ENSP00000365402.5:n.*247C=
ENST00000376228.9:c.*247C= ENSP00000365402.5:n.*247C=
ENST00000376237.8:c.*935C= ENSP00000365412.4:n.*935C=
ENST00000383329.7:c.*247C= ENSP00000372819.3:n.*247C=
ENST00000466892.5:n.581C=
ENST00000470363.5:n.1106C=
ENST00000487245.5:n.1707C=
NM_002117.5:c.*247C= NP_002108.4:n.*247C=
NM_002117.6:c.*247C= MANE Select NP_002108.4:n.*247C=