Canonical Allele Identifier: CA363319566
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761160954
gnomAD v3: 6-31269978-T-C
gnomAD v4: 6-31269978-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269978T>C , CM000668.2:g.31269978T>C GRCh38
NC_000006.11:g.31237755T>C , CM000668.1:g.31237755T>C GRCh37
NC_000006.10:g.31345734T>C NCBI36
NG_029422.2:g.7154A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1003A>G MANE Select ENSP00000365402.5:p.Arg335Gly
ENST00000376228.9:c.1003A>G ENSP00000365402.5:p.Arg335Gly
ENST00000376237.8:c.*590A>G ENSP00000365412.4:n.*590A>G
ENST00000383329.7:c.1003A>G ENSP00000372819.3:p.Arg335Gly
ENST00000470363.5:n.321A>G
ENST00000487245.5:n.1362A>G
NM_002117.5:c.1003A>G NP_002108.4:p.Arg335Gly
NM_002117.6:c.1003A>G MANE Select NP_002108.4:p.Arg335Gly