Canonical Allele Identifier: CA1619078558
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269926G= , CM000668.2:g.31269926G= GRCh38
NC_000006.11:g.31237703G= , CM000668.1:g.31237703G= GRCh37
NC_000006.10:g.31345682G= NCBI36
NG_029422.2:g.7206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+40C= MANE Select ENSP00000365402.5:n.1015+40C=
ENST00000376228.9:c.1015+40C= ENSP00000365402.5:n.1015+40C=
ENST00000376237.8:c.*602+40C= ENSP00000365412.4:n.*602+40C=
ENST00000383329.7:c.1015+40C= ENSP00000372819.3:n.1015+40C=
ENST00000470363.5:n.373C=
ENST00000487245.5:n.1374+40C=
NM_002117.5:c.1015+40C= NP_002108.4:n.1015+40C=
NM_002117.6:c.1015+40C= MANE Select NP_002108.4:n.1015+40C=
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