Canonical Allele Identifier: CA1619077266
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269059A= , CM000668.2:g.31269059A= GRCh38
NC_000006.11:g.31236836A= , CM000668.1:g.31236836A= GRCh37
NC_000006.10:g.31344815A= NCBI36
NG_029422.2:g.8073T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*110T= MANE Select ENSP00000365402.5:n.*110T=
ENST00000376228.9:c.*110T= ENSP00000365402.5:n.*110T=
ENST00000376237.8:c.*798T= ENSP00000365412.4:n.*798T=
ENST00000383329.7:c.*110T= ENSP00000372819.3:n.*110T=
ENST00000466892.5:n.444T=
ENST00000470363.5:n.969T=
ENST00000487245.5:n.1570T=
NM_002117.5:c.*110T= NP_002108.4:n.*110T=
NM_002117.6:c.*110T= MANE Select NP_002108.4:n.*110T=