Canonical Allele Identifier: CA1619077178
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268939C= , CM000668.2:g.31268939C= GRCh38
NC_000006.11:g.31236716C= , CM000668.1:g.31236716C= GRCh37
NC_000006.10:g.31344695C= NCBI36
NG_029422.2:g.8193G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*230G= MANE Select ENSP00000365402.5:n.*230G=
ENST00000376228.9:c.*230G= ENSP00000365402.5:n.*230G=
ENST00000376237.8:c.*918G= ENSP00000365412.4:n.*918G=
ENST00000383329.7:c.*230G= ENSP00000372819.3:n.*230G=
ENST00000466892.5:n.564G=
ENST00000470363.5:n.1089G=
ENST00000487245.5:n.1690G=
NM_002117.5:c.*230G= NP_002108.4:n.*230G=
NM_002117.6:c.*230G= MANE Select NP_002108.4:n.*230G=