Canonical Allele Identifier: CA1619080064
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270654G= , CM000668.2:g.31270654G= GRCh38
NC_000006.11:g.31238431G= , CM000668.1:g.31238431G= GRCh37
NC_000006.10:g.31346410G= NCBI36
NG_029422.2:g.6478C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-169C= MANE Select ENSP00000365402.5:n.620-169C=
ENST00000376228.9:c.620-169C= ENSP00000365402.5:n.620-169C=
ENST00000376237.8:c.*207-169C= ENSP00000365412.4:n.*207-169C=
ENST00000383329.7:c.620-169C= ENSP00000372819.3:n.620-169C=
ENST00000415537.1:c.618-169C=
ENST00000487245.5:n.979-169C=
ENST00000495835.1:n.809-169C=
NM_002117.5:c.620-169C= NP_002108.4:n.620-169C=
NM_002117.6:c.620-169C= MANE Select NP_002108.4:n.620-169C=
Search 100 bp 5'
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