Canonical Allele Identifier: CA1619077390
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269167T= , CM000668.2:g.31269167T= GRCh38
NC_000006.11:g.31236944T= , CM000668.1:g.31236944T= GRCh37
NC_000006.10:g.31344923T= NCBI36
NG_029422.2:g.7965A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*2A= MANE Select ENSP00000365402.5:n.*2A=
ENST00000376228.9:c.*2A= ENSP00000365402.5:n.*2A=
ENST00000376237.8:c.*690A= ENSP00000365412.4:n.*690A=
ENST00000383329.7:c.*2A= ENSP00000372819.3:n.*2A=
ENST00000466892.5:n.336A=
ENST00000470363.5:n.861A=
ENST00000487245.5:n.1462A=
NM_002117.5:c.*2A= NP_002108.4:n.*2A=
NM_002117.6:c.*2A= MANE Select NP_002108.4:n.*2A=
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Search 100 bp 3'