Canonical Allele Identifier: CA566336278
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1352719891
gnomAD v2: 6-31236908-A-C
gnomAD v3: 6-31269131-A-C
gnomAD v4: 6-31269131-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269131A>C , CM000668.2:g.31269131A>C GRCh38
NC_000006.11:g.31236908A>C , CM000668.1:g.31236908A>C GRCh37
NC_000006.10:g.31344887A>C NCBI36
NG_029422.2:g.8001T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*38T>G MANE Select ENSP00000365402.5:n.*38T>G
ENST00000376228.9:c.*38T>G ENSP00000365402.5:n.*38T>G
ENST00000376237.8:c.*726T>G ENSP00000365412.4:n.*726T>G
ENST00000383329.7:c.*38T>G ENSP00000372819.3:n.*38T>G
ENST00000466892.5:n.372T>G
ENST00000470363.5:n.897T>G
ENST00000487245.5:n.1498T>G
NM_002117.5:c.*38T>G NP_002108.4:n.*38T>G
NM_002117.6:c.*38T>G MANE Select NP_002108.4:n.*38T>G