Canonical Allele Identifier: CA1619077840
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269420C= , CM000668.2:g.31269420C= GRCh38
NC_000006.11:g.31237197C= , CM000668.1:g.31237197C= GRCh37
NC_000006.10:g.31345176C= NCBI36
NG_029422.2:g.7712G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1049-35G= MANE Select ENSP00000365402.5:n.1049-35G=
ENST00000376228.9:c.1049-35G= ENSP00000365402.5:n.1049-35G=
ENST00000376237.8:c.*636-35G= ENSP00000365412.4:n.*636-35G=
ENST00000383329.7:c.1067-35G= ENSP00000372819.3:n.1067-35G=
ENST00000466892.5:n.247G=
ENST00000470363.5:n.807-35G=
ENST00000487245.5:n.1408-35G=
NM_002117.5:c.1049-35G= NP_002108.4:n.1049-35G=
NM_002117.6:c.1049-35G= MANE Select NP_002108.4:n.1049-35G=
Search 100 bp 5'
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