Canonical Allele Identifier: CA1619077172
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268932C= , CM000668.2:g.31268932C= GRCh38
NC_000006.11:g.31236709C= , CM000668.1:g.31236709C= GRCh37
NC_000006.10:g.31344688C= NCBI36
NG_029422.2:g.8200G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*237G= MANE Select ENSP00000365402.5:n.*237G=
ENST00000376228.9:c.*237G= ENSP00000365402.5:n.*237G=
ENST00000376237.8:c.*925G= ENSP00000365412.4:n.*925G=
ENST00000383329.7:c.*237G= ENSP00000372819.3:n.*237G=
ENST00000466892.5:n.571G=
ENST00000470363.5:n.1096G=
ENST00000487245.5:n.1697G=
NM_002117.5:c.*237G= NP_002108.4:n.*237G=
NM_002117.6:c.*237G= MANE Select NP_002108.4:n.*237G=