Canonical Allele Identifier: CA1619077158
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268913T= , CM000668.2:g.31268913T= GRCh38
NC_000006.11:g.31236690T= , CM000668.1:g.31236690T= GRCh37
NC_000006.10:g.31344669T= NCBI36
NG_029422.2:g.8219A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*256A= MANE Select ENSP00000365402.5:n.*256A=
ENST00000376228.9:c.*256A= ENSP00000365402.5:n.*256A=
ENST00000376237.8:c.*944A= ENSP00000365412.4:n.*944A=
ENST00000383329.7:c.*256A= ENSP00000372819.3:n.*256A=
ENST00000466892.5:n.590A=
ENST00000470363.5:n.1115A=
ENST00000487245.5:n.1716A=
NM_002117.5:c.*256A= NP_002108.4:n.*256A=
NM_002117.6:c.*256A= MANE Select NP_002108.4:n.*256A=