Canonical Allele Identifier: CA1619077195
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268968C= , CM000668.2:g.31268968C= GRCh38
NC_000006.11:g.31236745C= , CM000668.1:g.31236745C= GRCh37
NC_000006.10:g.31344724C= NCBI36
NG_029422.2:g.8164G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*201G= MANE Select ENSP00000365402.5:n.*201G=
ENST00000376228.9:c.*201G= ENSP00000365402.5:n.*201G=
ENST00000376237.8:c.*889G= ENSP00000365412.4:n.*889G=
ENST00000383329.7:c.*201G= ENSP00000372819.3:n.*201G=
ENST00000466892.5:n.535G=
ENST00000470363.5:n.1060G=
ENST00000487245.5:n.1661G=
NM_002117.5:c.*201G= NP_002108.4:n.*201G=
NM_002117.6:c.*201G= MANE Select NP_002108.4:n.*201G=