Canonical Allele Identifier: CA136866943
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860503
gnomAD v4: 6-31271187-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271187G>C , CM000668.2:g.31271187G>C GRCh38
NC_000006.11:g.31238964G>C , CM000668.1:g.31238964G>C GRCh37
NC_000006.10:g.31346943G>C NCBI36
NG_029422.2:g.5945C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.505C>G MANE Select ENSP00000365402.5:p.Arg169Gly
ENST00000376228.9:c.505C>G ENSP00000365402.5:p.Arg169Gly
ENST00000376237.8:c.*92C>G ENSP00000365412.4:n.*92C>G
ENST00000383329.7:c.505C>G ENSP00000372819.3:p.Arg169Gly
ENST00000415537.1:c.503C>G
ENST00000484378.1:n.774C>G
ENST00000487245.5:n.864C>G
ENST00000495835.1:n.694C>G
NM_002117.5:c.505C>G NP_002108.4:p.Arg169Gly
NM_002117.6:c.505C>G MANE Select NP_002108.4:p.Arg169Gly