Canonical Allele Identifier: CA1619077194
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268967T= , CM000668.2:g.31268967T= GRCh38
NC_000006.11:g.31236744T= , CM000668.1:g.31236744T= GRCh37
NC_000006.10:g.31344723T= NCBI36
NG_029422.2:g.8165A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*202A= MANE Select ENSP00000365402.5:n.*202A=
ENST00000376228.9:c.*202A= ENSP00000365402.5:n.*202A=
ENST00000376237.8:c.*890A= ENSP00000365412.4:n.*890A=
ENST00000383329.7:c.*202A= ENSP00000372819.3:n.*202A=
ENST00000466892.5:n.536A=
ENST00000470363.5:n.1061A=
ENST00000487245.5:n.1662A=
NM_002117.5:c.*202A= NP_002108.4:n.*202A=
NM_002117.6:c.*202A= MANE Select NP_002108.4:n.*202A=