Canonical Allele Identifier: CA1619077924
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269470A= , CM000668.2:g.31269470A= GRCh38
NC_000006.11:g.31237247A= , CM000668.1:g.31237247A= GRCh37
NC_000006.10:g.31345226A= NCBI36
NG_029422.2:g.7662T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1048+23T= MANE Select ENSP00000365402.5:n.1048+23T=
ENST00000376228.9:c.1048+23T= ENSP00000365402.5:n.1048+23T=
ENST00000376237.8:c.*635+23T= ENSP00000365412.4:n.*635+23T=
ENST00000383329.7:c.1066+23T= ENSP00000372819.3:n.1066+23T=
ENST00000466892.5:n.197T=
ENST00000470363.5:n.806+23T=
ENST00000487245.5:n.1407+23T=
NM_002117.5:c.1048+23T= NP_002108.4:n.1048+23T=
NM_002117.6:c.1048+23T= MANE Select NP_002108.4:n.1048+23T=
Search 100 bp 5'
Search 100 bp 3'