Canonical Allele Identifier: CA1619078303
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761140917
gnomAD v4: 6-31269710-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269710C>G , CM000668.2:g.31269710C>G GRCh38
NC_000006.11:g.31237487C>G , CM000668.1:g.31237487C>G GRCh37
NC_000006.10:g.31345466C>G NCBI36
NG_029422.2:g.7422G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-185G>C MANE Select ENSP00000365402.5:n.1016-185G>C
ENST00000376228.9:c.1016-185G>C ENSP00000365402.5:n.1016-185G>C
ENST00000376237.8:c.*603-185G>C ENSP00000365412.4:n.*603-185G>C
ENST00000383329.7:c.1016-167G>C ENSP00000372819.3:n.1016-167G>C
ENST00000470363.5:n.589G>C
ENST00000487245.5:n.1375-185G>C
NM_002117.5:c.1016-185G>C NP_002108.4:n.1016-185G>C
NM_002117.6:c.1016-185G>C MANE Select NP_002108.4:n.1016-185G>C