Canonical Allele Identifier: CA2677949165
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268946-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268946T>C , CM000668.2:g.31268946T>C GRCh38
NC_000006.11:g.31236723T>C , CM000668.1:g.31236723T>C GRCh37
NC_000006.10:g.31344702T>C NCBI36
NG_029422.2:g.8186A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*223A>G MANE Select ENSP00000365402.5:n.*223A>G
ENST00000376228.9:c.*223A>G ENSP00000365402.5:n.*223A>G
ENST00000376237.8:c.*911A>G ENSP00000365412.4:n.*911A>G
ENST00000383329.7:c.*223A>G ENSP00000372819.3:n.*223A>G
ENST00000466892.5:n.557A>G
ENST00000470363.5:n.1082A>G
ENST00000487245.5:n.1683A>G
NM_002117.5:c.*223A>G NP_002108.4:n.*223A>G
NM_002117.6:c.*223A>G MANE Select NP_002108.4:n.*223A>G