ClinVar Variation:
COSMIC:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00001747 (AFR)
Genomes Max Group AF
0.00003252 (AFR)
Exomes Max Group AF
8.4e-7 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154157C>T , CM000681.2:g.55154157C>T | GRCh38 |
| NC_000019.9:g.55665525C>T , CM000681.1:g.55665525C>T | GRCh37 |
| NC_000019.8:g.60357337C>T | NCBI36 |
| NG_007866.2:g.8576G>A , LRG_432:g.8576G>A | |
| NG_011829.2:g.82G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.422G>A MANE Select | ENSP00000341838.5:p.Arg141Gln | |
| ENST00000665070.1:c.455G>A | ENSP00000499482.1:p.Arg152Gln | |
| ENST00000344887.9:c.422G>A | ENSP00000341838.5:p.Arg141Gln | |
| ENST00000585806.5:n.421G>A | ||
| ENST00000586669.5:n.430G>A | ||
| ENST00000588882.1:c.347G>A | ENSP00000466729.1:p.Arg116Gln | |
| ENST00000589864.1:n.250G>A | ||
| NM_000363.4:c.422G>A , LRG_432t1:c.422G>A | NP_000354.4:p.Arg141Gln | |
| NM_000363.5:c.422G>A MANE Select | NP_000354.4:p.Arg141Gln |