Canonical Allele Identifier: CA1619079166
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270167G= , CM000668.2:g.31270167G= GRCh38
NC_000006.11:g.31237944G= , CM000668.1:g.31237944G= GRCh37
NC_000006.10:g.31345923G= NCBI36
NG_029422.2:g.6965C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+43C= MANE Select ENSP00000365402.5:n.895+43C=
ENST00000376228.9:c.895+43C= ENSP00000365402.5:n.895+43C=
ENST00000376237.8:c.*482+43C= ENSP00000365412.4:n.*482+43C=
ENST00000383329.7:c.895+43C= ENSP00000372819.3:n.895+43C=
ENST00000470363.5:n.213+43C=
ENST00000487245.5:n.1254+43C=
NM_002117.5:c.895+43C= NP_002108.4:n.895+43C=
NM_002117.6:c.895+43C= MANE Select NP_002108.4:n.895+43C=
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