Canonical Allele Identifier: CA1619080634
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271465C= , CM000668.2:g.31271465C= GRCh38
NC_000006.11:g.31239242C= , CM000668.1:g.31239242C= GRCh37
NC_000006.10:g.31347221C= NCBI36
NG_029422.2:g.5667G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-117G= MANE Select ENSP00000365402.5:n.344-117G=
ENST00000376228.9:c.344-117G= ENSP00000365402.5:n.344-117G=
ENST00000376237.8:c.344-134G= ENSP00000365412.4:n.344-134G=
ENST00000383329.7:c.344-117G= ENSP00000372819.3:n.344-117G=
ENST00000415537.1:c.342-117G=
ENST00000484378.1:n.496G=
ENST00000487245.5:n.586G=
ENST00000495835.1:n.533-117G=
NM_002117.5:c.344-117G= NP_002108.4:n.344-117G=
NM_002117.6:c.344-117G= MANE Select NP_002108.4:n.344-117G=
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