Canonical Allele Identifier: CA1619078485
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269866A= , CM000668.2:g.31269866A= GRCh38
NC_000006.11:g.31237643A= , CM000668.1:g.31237643A= GRCh37
NC_000006.10:g.31345622A= NCBI36
NG_029422.2:g.7266T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+100T= MANE Select ENSP00000365402.5:n.1015+100T=
ENST00000376228.9:c.1015+100T= ENSP00000365402.5:n.1015+100T=
ENST00000376237.8:c.*602+100T= ENSP00000365412.4:n.*602+100T=
ENST00000383329.7:c.1015+100T= ENSP00000372819.3:n.1015+100T=
ENST00000470363.5:n.433T=
ENST00000487245.5:n.1374+100T=
NM_002117.5:c.1015+100T= NP_002108.4:n.1015+100T=
NM_002117.6:c.1015+100T= MANE Select NP_002108.4:n.1015+100T=