Linked Data
ClinVar Variation Id:
417961
dbSNP Id:
rs1060499616
gnomAD v4:
21-34880568-C-T
PubMed:
PMID:10508512
ERepo:
CA16616941/MONDO:0011071/008
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34880568C>T , CM000683.2:g.34880568C>T | GRCh38 |
| NC_000021.8:g.36252865C>T , CM000683.1:g.36252865C>T | GRCh37 |
| NC_000021.7:g.35174735C>T | NCBI36 |
| NG_011402.2:g.1109144G>A , LRG_482:g.1109144G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000675419.1:c.497G>A MANE Select | ENSP00000501943.1:p.Arg166Gln | |
| ENST00000300305.7:c.497G>A | ENSP00000300305.3:p.Arg166Gln | |
| ENST00000344691.8:c.416G>A | ENSP00000340690.4:p.Arg139Gln | |
| ENST00000358356.9:c.416G>A | ENSP00000351123.5:p.Arg139Gln | |
| ENST00000399237.6:c.461G>A | ENSP00000382182.2:p.Arg154Gln | |
| ENST00000399240.5:c.416G>A | ENSP00000382184.1:p.Arg139Gln | |
| ENST00000437180.5:c.497G>A | ENSP00000409227.1:p.Arg166Gln | |
| ENST00000482318.5:c.*87G>A | ENSP00000477067.1:n.*87G>A | |
| NM_001001890.2:c.416G>A | NP_001001890.1:p.Arg139Gln | |
| NM_001122607.1:c.416G>A | NP_001116079.1:p.Arg139Gln | |
| NM_001754.4:c.497G>A , LRG_482t1:c.497G>A | NP_001745.2:p.Arg166Gln | |
| XM_005261068.3:c.461G>A | XP_005261125.1:p.Arg154Gln | |
| XM_005261069.3:c.497G>A | XP_005261126.1:p.Arg166Gln | |
| XM_011529766.1:c.497G>A | XP_011528068.1:p.Arg166Gln | |
| XM_011529767.1:c.458G>A | XP_011528069.1:p.Arg153Gln | |
| XM_011529768.1:c.458G>A | XP_011528070.1:p.Arg153Gln | |
| XM_011529770.1:c.497G>A | XP_011528072.1:p.Arg166Gln | |
| XR_937576.1:n.676G>A | ||
| XM_005261069.4:c.497G>A | XP_005261126.1:p.Arg166Gln | |
| XM_011529766.2:c.497G>A | XP_011528068.1:p.Arg166Gln | |
| XM_011529767.2:c.458G>A | XP_011528069.1:p.Arg153Gln | |
| XM_011529768.2:c.458G>A | XP_011528070.1:p.Arg153Gln | |
| XM_011529770.2:c.497G>A | XP_011528072.1:p.Arg166Gln | |
| XM_017028487.1:c.344G>A | XP_016883976.1:p.Arg115Gln | |
| XR_937576.2:n.723G>A | ||
| NM_001001890.3:c.416G>A | NP_001001890.1:p.Arg139Gln | |
| NM_001122607.2:c.416G>A | NP_001116079.1:p.Arg139Gln | |
| NM_001754.5:c.497G>A MANE Select | NP_001745.2:p.Arg166Gln |