Canonical Allele Identifier: CA136868417
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41540717
gnomAD v4: 6-31271530-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271530G>C , CM000668.2:g.31271530G>C GRCh38
NC_000006.11:g.31239307G>C , CM000668.1:g.31239307G>C GRCh37
NC_000006.10:g.31347286G>C NCBI36
NG_029422.2:g.5602C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+69C>G MANE Select ENSP00000365402.5:n.343+69C>G
ENST00000376228.9:c.343+69C>G ENSP00000365402.5:n.343+69C>G
ENST00000376237.8:c.343+69C>G ENSP00000365412.4:n.343+69C>G
ENST00000383329.7:c.343+69C>G ENSP00000372819.3:n.343+69C>G
ENST00000415537.1:c.341+69C>G
ENST00000484378.1:n.431C>G
ENST00000487245.5:n.521C>G
ENST00000495835.1:n.532+69C>G
NM_002117.5:c.343+69C>G NP_002108.4:n.343+69C>G
NM_002117.6:c.343+69C>G MANE Select NP_002108.4:n.343+69C>G