Canonical Allele Identifier: CA1619078329
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269727C= , CM000668.2:g.31269727C= GRCh38
NC_000006.11:g.31237504C= , CM000668.1:g.31237504C= GRCh37
NC_000006.10:g.31345483C= NCBI36
NG_029422.2:g.7405G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-202G= MANE Select ENSP00000365402.5:n.1016-202G=
ENST00000376228.9:c.1016-202G= ENSP00000365402.5:n.1016-202G=
ENST00000376237.8:c.*603-202G= ENSP00000365412.4:n.*603-202G=
ENST00000383329.7:c.1016-184G= ENSP00000372819.3:n.1016-184G=
ENST00000470363.5:n.572G=
ENST00000487245.5:n.1375-202G=
NM_002117.5:c.1016-202G= NP_002108.4:n.1016-202G=
NM_002117.6:c.1016-202G= MANE Select NP_002108.4:n.1016-202G=