Canonical Allele Identifier: CA566336272
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1459822162
gnomAD v2: 6-31236832-C-G
gnomAD v3: 6-31269055-C-G
gnomAD v4: 6-31269055-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269055C>G , CM000668.2:g.31269055C>G GRCh38
NC_000006.11:g.31236832C>G , CM000668.1:g.31236832C>G GRCh37
NC_000006.10:g.31344811C>G NCBI36
NG_029422.2:g.8077G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*114G>C MANE Select ENSP00000365402.5:n.*114G>C
ENST00000376228.9:c.*114G>C ENSP00000365402.5:n.*114G>C
ENST00000376237.8:c.*802G>C ENSP00000365412.4:n.*802G>C
ENST00000383329.7:c.*114G>C ENSP00000372819.3:n.*114G>C
ENST00000466892.5:n.448G>C
ENST00000470363.5:n.973G>C
ENST00000487245.5:n.1574G>C
NM_002117.5:c.*114G>C NP_002108.4:n.*114G>C
NM_002117.6:c.*114G>C MANE Select NP_002108.4:n.*114G>C