Canonical Allele Identifier: CA1619077127
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268868A= , CM000668.2:g.31268868A= GRCh38
NC_000006.11:g.31236645A= , CM000668.1:g.31236645A= GRCh37
NC_000006.10:g.31344624A= NCBI36
NG_029422.2:g.8264T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*301T= MANE Select ENSP00000365402.5:n.*301T=
ENST00000376228.9:c.*301T= ENSP00000365402.5:n.*301T=
ENST00000376237.8:c.*989T= ENSP00000365412.4:n.*989T=
ENST00000383329.7:c.*301T= ENSP00000372819.3:n.*301T=
ENST00000466892.5:n.635T=
ENST00000470363.5:n.1160T=
ENST00000487245.5:n.1761T=
NM_002117.5:c.*301T= NP_002108.4:n.*301T=
NM_002117.6:c.*301T= MANE Select NP_002108.4:n.*301T=
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