Canonical Allele Identifier: CA823860875
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1463826154
gnomAD v3: 6-31269148-A-G
gnomAD v4: 6-31269148-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269148A>G , CM000668.2:g.31269148A>G GRCh38
NC_000006.11:g.31236925A>G , CM000668.1:g.31236925A>G GRCh37
NC_000006.10:g.31344904A>G NCBI36
NG_029422.2:g.7984T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*21T>C MANE Select ENSP00000365402.5:n.*21T>C
ENST00000376228.9:c.*21T>C ENSP00000365402.5:n.*21T>C
ENST00000376237.8:c.*709T>C ENSP00000365412.4:n.*709T>C
ENST00000383329.7:c.*21T>C ENSP00000372819.3:n.*21T>C
ENST00000466892.5:n.355T>C
ENST00000470363.5:n.880T>C
ENST00000487245.5:n.1481T>C
NM_002117.5:c.*21T>C NP_002108.4:n.*21T>C
NM_002117.6:c.*21T>C MANE Select NP_002108.4:n.*21T>C