Canonical Allele Identifier: CA363325530
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271184-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271184T>C , CM000668.2:g.31271184T>C GRCh38
NC_000006.11:g.31238961T>C , CM000668.1:g.31238961T>C GRCh37
NC_000006.10:g.31346940T>C NCBI36
NG_029422.2:g.5948A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.508A>G MANE Select ENSP00000365402.5:p.Lys170Glu
ENST00000376228.9:c.508A>G ENSP00000365402.5:p.Lys170Glu
ENST00000376237.8:c.*95A>G ENSP00000365412.4:n.*95A>G
ENST00000383329.7:c.508A>G ENSP00000372819.3:p.Lys170Glu
ENST00000415537.1:c.506A>G
ENST00000484378.1:n.777A>G
ENST00000487245.5:n.867A>G
ENST00000495835.1:n.697A>G
NM_002117.5:c.508A>G NP_002108.4:p.Lys170Glu
NM_002117.6:c.508A>G MANE Select NP_002108.4:p.Lys170Glu