Canonical Allele Identifier: CA1619077198
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268981C= , CM000668.2:g.31268981C= GRCh38
NC_000006.11:g.31236758C= , CM000668.1:g.31236758C= GRCh37
NC_000006.10:g.31344737C= NCBI36
NG_029422.2:g.8151G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*188G= MANE Select ENSP00000365402.5:n.*188G=
ENST00000376228.9:c.*188G= ENSP00000365402.5:n.*188G=
ENST00000376237.8:c.*876G= ENSP00000365412.4:n.*876G=
ENST00000383329.7:c.*188G= ENSP00000372819.3:n.*188G=
ENST00000466892.5:n.522G=
ENST00000470363.5:n.1047G=
ENST00000487245.5:n.1648G=
NM_002117.5:c.*188G= NP_002108.4:n.*188G=
NM_002117.6:c.*188G= MANE Select NP_002108.4:n.*188G=