Canonical Allele Identifier: CA363327200
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860444
gnomAD v3: 6-31271333-T-A
gnomAD v4: 6-31271333-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271333T>A , CM000668.2:g.31271333T>A GRCh38
NC_000006.11:g.31239110T>A , CM000668.1:g.31239110T>A GRCh37
NC_000006.10:g.31347089T>A NCBI36
NG_029422.2:g.5799A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.359A>T MANE Select ENSP00000365402.5:p.Gln120Leu
ENST00000376228.9:c.359A>T ENSP00000365402.5:p.Gln120Leu
ENST00000376237.8:c.344-2A>T ENSP00000365412.4:n.344-2A>T
ENST00000383329.7:c.359A>T ENSP00000372819.3:p.Gln120Leu
ENST00000415537.1:c.357A>T
ENST00000484378.1:n.628A>T
ENST00000487245.5:n.718A>T
ENST00000495835.1:n.548A>T
NM_002117.5:c.359A>T NP_002108.4:p.Gln120Leu
NM_002117.6:c.359A>T MANE Select NP_002108.4:p.Gln120Leu