Canonical Allele Identifier: CA1619077192
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268964T= , CM000668.2:g.31268964T= GRCh38
NC_000006.11:g.31236741T= , CM000668.1:g.31236741T= GRCh37
NC_000006.10:g.31344720T= NCBI36
NG_029422.2:g.8168A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*205A= MANE Select ENSP00000365402.5:n.*205A=
ENST00000376228.9:c.*205A= ENSP00000365402.5:n.*205A=
ENST00000376237.8:c.*893A= ENSP00000365412.4:n.*893A=
ENST00000383329.7:c.*205A= ENSP00000372819.3:n.*205A=
ENST00000466892.5:n.539A=
ENST00000470363.5:n.1064A=
ENST00000487245.5:n.1665A=
NM_002117.5:c.*205A= NP_002108.4:n.*205A=
NM_002117.6:c.*205A= MANE Select NP_002108.4:n.*205A=
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