Canonical Allele Identifier: CA363319555
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269974-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269974T>C , CM000668.2:g.31269974T>C GRCh38
NC_000006.11:g.31237751T>C , CM000668.1:g.31237751T>C GRCh37
NC_000006.10:g.31345730T>C NCBI36
NG_029422.2:g.7158A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1007A>G MANE Select ENSP00000365402.5:p.Lys336Arg
ENST00000376228.9:c.1007A>G ENSP00000365402.5:p.Lys336Arg
ENST00000376237.8:c.*594A>G ENSP00000365412.4:n.*594A>G
ENST00000383329.7:c.1007A>G ENSP00000372819.3:p.Lys336Arg
ENST00000470363.5:n.325A>G
ENST00000487245.5:n.1366A>G
NM_002117.5:c.1007A>G NP_002108.4:p.Lys336Arg
NM_002117.6:c.1007A>G MANE Select NP_002108.4:p.Lys336Arg