Canonical Allele Identifier: CA1619080846
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271728G= , CM000668.2:g.31271728G= GRCh38
NC_000006.11:g.31239505G= , CM000668.1:g.31239505G= GRCh37
NC_000006.10:g.31347484G= NCBI36
NG_029422.2:g.5404C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.214C= MANE Select ENSP00000365402.5:p.Arg72=
ENST00000376228.9:c.214C= ENSP00000365402.5:p.Arg72=
ENST00000376237.8:c.214C= ENSP00000365412.4:p.Arg72=
ENST00000383329.7:c.214C= ENSP00000372819.3:p.Arg72=
ENST00000415537.1:c.212C=
ENST00000484378.1:n.233C=
ENST00000487245.5:n.323C=
ENST00000495835.1:n.403C=
NM_002117.5:c.214C= NP_002108.4:p.Arg72=
NM_002117.6:c.214C= MANE Select NP_002108.4:p.Arg72=