Canonical Allele Identifier: CA3710566
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860563
gnomAD v2: 6-31238140-G-T
gnomAD v4: 6-31270363-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270363G>T , CM000668.2:g.31270363G>T GRCh38
NC_000006.11:g.31238140G>T , CM000668.1:g.31238140G>T GRCh37
NC_000006.10:g.31346119G>T NCBI36
NG_029422.2:g.6769C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.742C>A MANE Select ENSP00000365402.5:p.Gln248Lys
ENST00000376228.9:c.742C>A ENSP00000365402.5:p.Gln248Lys
ENST00000376237.8:c.*329C>A ENSP00000365412.4:n.*329C>A
ENST00000383329.7:c.742C>A ENSP00000372819.3:p.Gln248Lys
ENST00000415537.1:c.665-32C>A
ENST00000470363.5:n.60C>A
ENST00000487245.5:n.1101C>A
ENST00000495835.1:n.931C>A
NM_002117.5:c.742C>A NP_002108.4:p.Gln248Lys
NM_002117.6:c.742C>A MANE Select NP_002108.4:p.Gln248Lys