Canonical Allele Identifier: CA1619077193
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761091261
gnomAD v3: 6-31268964-T-C
gnomAD v4: 6-31268964-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268964T>C , CM000668.2:g.31268964T>C GRCh38
NC_000006.11:g.31236741T>C , CM000668.1:g.31236741T>C GRCh37
NC_000006.10:g.31344720T>C NCBI36
NG_029422.2:g.8168A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*205A>G MANE Select ENSP00000365402.5:n.*205A>G
ENST00000376228.9:c.*205A>G ENSP00000365402.5:n.*205A>G
ENST00000376237.8:c.*893A>G ENSP00000365412.4:n.*893A>G
ENST00000383329.7:c.*205A>G ENSP00000372819.3:n.*205A>G
ENST00000466892.5:n.539A>G
ENST00000470363.5:n.1064A>G
ENST00000487245.5:n.1665A>G
NM_002117.5:c.*205A>G NP_002108.4:n.*205A>G
NM_002117.6:c.*205A>G MANE Select NP_002108.4:n.*205A>G