Canonical Allele Identifier: CA1619077196
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268969G= , CM000668.2:g.31268969G= GRCh38
NC_000006.11:g.31236746G= , CM000668.1:g.31236746G= GRCh37
NC_000006.10:g.31344725G= NCBI36
NG_029422.2:g.8163C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*200C= MANE Select ENSP00000365402.5:n.*200C=
ENST00000376228.9:c.*200C= ENSP00000365402.5:n.*200C=
ENST00000376237.8:c.*888C= ENSP00000365412.4:n.*888C=
ENST00000383329.7:c.*200C= ENSP00000372819.3:n.*200C=
ENST00000466892.5:n.534C=
ENST00000470363.5:n.1059C=
ENST00000487245.5:n.1660C=
NM_002117.5:c.*200C= NP_002108.4:n.*200C=
NM_002117.6:c.*200C= MANE Select NP_002108.4:n.*200C=
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