Canonical Allele Identifier: CA1619077649
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269319C= , CM000668.2:g.31269319C= GRCh38
NC_000006.11:g.31237096C= , CM000668.1:g.31237096C= GRCh37
NC_000006.10:g.31345075C= NCBI36
NG_029422.2:g.7813G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+19G= MANE Select ENSP00000365402.5:n.1096+19G=
ENST00000376228.9:c.1096+19G= ENSP00000365402.5:n.1096+19G=
ENST00000376237.8:c.*683+19G= ENSP00000365412.4:n.*683+19G=
ENST00000383329.7:c.1114+19G= ENSP00000372819.3:n.1114+19G=
ENST00000466892.5:n.329+19G=
ENST00000470363.5:n.854+19G=
ENST00000487245.5:n.1455+19G=
NM_002117.5:c.1096+19G= NP_002108.4:n.1096+19G=
NM_002117.6:c.1096+19G= MANE Select NP_002108.4:n.1096+19G=
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