Canonical Allele Identifier: CA12292563
Gene: HLA-C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2394961

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269250C>T , CM000668.2:g.31269250C>T GRCh38
NC_000006.11:g.31237027C>T , CM000668.1:g.31237027C>T GRCh37
NC_000006.10:g.31345006C>T NCBI36
NG_029422.2:g.7882G>A

Transcript Alleles

HGVS Amino-acid change
NM_002117.5:c.1097-77G>A VV NP_002108.4:p.=
ENST00000376228.9:c.1097-77G>A ENSP00000365402.5:p.=
ENST00000376237.8:c.*684-77G>A ENSP00000365412.4:p.=
ENST00000383329.7:c.1115-77G>A ENSP00000372819.3:p.=
ENST00000466892.5:n.330-77G>A
ENST00000470363.5:n.855-77G>A
ENST00000487245.5:n.1456-77G>A