Canonical Allele Identifier: CA136867298
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860474
gnomAD v4: 6-31271258-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271258T>C , CM000668.2:g.31271258T>C GRCh38
NC_000006.11:g.31239035T>C , CM000668.1:g.31239035T>C GRCh37
NC_000006.10:g.31347014T>C NCBI36
NG_029422.2:g.5874A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.434A>G MANE Select ENSP00000365402.5:p.Lys145Arg
ENST00000376228.9:c.434A>G ENSP00000365402.5:p.Lys145Arg
ENST00000376237.8:c.*21A>G ENSP00000365412.4:n.*21A>G
ENST00000383329.7:c.434A>G ENSP00000372819.3:p.Lys145Arg
ENST00000415537.1:c.432A>G
ENST00000484378.1:n.703A>G
ENST00000487245.5:n.793A>G
ENST00000495835.1:n.623A>G
NM_002117.5:c.434A>G NP_002108.4:p.Lys145Arg
NM_002117.6:c.434A>G MANE Select NP_002108.4:p.Lys145Arg