Linked Data
ClinVar Variation Id:
38993
dbSNP Id:
rs281865495
ExAC:
16:66551095 T / C
gnomAD v2:
16-66551095-T-C
gnomAD v3:
16-66517192-T-C
gnomAD v4:
16-66517192-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.66517192T>C , CM000678.2:g.66517192T>C | GRCh38 |
| NC_000016.9:g.66551095T>C , CM000678.1:g.66551095T>C | GRCh37 |
| NC_000016.8:g.65108596T>C | NCBI36 |
| NG_016862.1:g.38221A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299697.12:c.394A>G | ENSP00000299697.9:p.Thr132Ala | |
| ENST00000417693.8:c.508A>G | ENSP00000407469.5:p.Thr170Ala | |
| ENST00000451102.7:c.469A>G | ENSP00000414334.4:p.Thr157Ala | |
| ENST00000527284.6:c.506A>G | ||
| ENST00000527800.6:c.271A>G | ENSP00000433770.1:p.Thr91Ala | |
| ENST00000544898.6:c.562A>G MANE Select | ENSP00000440898.2:p.Thr188Ala | |
| ENST00000567357.6:c.*420A>G | ENSP00000457959.2:n.*420A>G | |
| ENST00000569718.6:c.357-3381A>G | ENSP00000464313.2:n.357-3381A>G | |
| ENST00000620035.5:c.375-3381A>G | ENSP00000483833.2:n.375-3381A>G | |
| ENST00000676538.1:c.145A>G | ||
| ENST00000676904.1:c.89+597A>G | ||
| ENST00000677379.1:c.203A>G | ENSP00000503672.1:n.203A>G | |
| ENST00000677420.1:c.271A>G | ENSP00000504648.1:p.Thr91Ala | |
| ENST00000677555.1:c.271A>G | ENSP00000503331.1:p.Thr91Ala | |
| ENST00000677715.1:c.271A>G | ENSP00000502950.1:p.Thr91Ala | |
| ENST00000678015.1:c.271A>G | ENSP00000502959.1:p.Thr91Ala | |
| ENST00000678297.1:c.271A>G | ENSP00000503472.1:p.Thr91Ala | |
| ENST00000678314.1:c.271A>G | ENSP00000504438.1:p.Thr91Ala | |
| ENST00000299697.11:c.562A>G | ENSP00000299697.8:p.Thr188Ala | |
| ENST00000417693.7:c.634A>G | ENSP00000407469.4:p.Thr212Ala | |
| ENST00000451102.6:c.688A>G | ENSP00000414334.3:p.Thr230Ala | |
| ENST00000525974.5:c.271A>G | ENSP00000434594.1:p.Thr91Ala | |
| ENST00000527284.5:c.469A>G | ENSP00000435312.1:p.Thr157Ala | |
| ENST00000527800.5:c.271A>G | ENSP00000433770.1:p.Thr91Ala | |
| ENST00000544898.5:c.562A>G | ENSP00000440898.2:p.Thr188Ala | |
| ENST00000545043.6:c.487A>G | ENSP00000438143.2:p.Thr163Ala | |
| ENST00000561527.5:n.121A>G | ||
| ENST00000561728.1:c.11A>G | ||
| ENST00000562552.5:n.378A>G | ||
| ENST00000563099.5:n.89A>G | ||
| ENST00000563369.6:c.271A>G | ENSP00000463560.1:p.Thr91Ala | |
| ENST00000563478.5:c.271A>G | ENSP00000462341.1:p.Thr91Ala | |
| ENST00000564792.1:n.217A>G | ||
| ENST00000564917.5:c.562A>G | ENSP00000455187.1:p.Thr188Ala | |
| ENST00000567357.5:c.*420A>G | ENSP00000457959.1:n.*420A>G | |
| ENST00000569718.5:c.344-3381A>G | ||
| ENST00000620035.4:c.508A>G | ENSP00000483833.1:p.Thr170Ala | |
| NM_001172643.1:c.469A>G | NP_001166114.1:p.Thr157Ala | |
| NM_001172644.1:c.487A>G | NP_001166115.1:p.Thr163Ala | |
| NM_001172645.1:c.508A>G | NP_001166116.1:p.Thr170Ala | |
| NM_001271934.1:c.415A>G | NP_001258863.1:p.Thr139Ala | |
| NM_001271935.1:c.357-3381A>G | NP_001258864.1:n.357-3381A>G | |
| NM_001272050.1:c.271A>G | NP_001258979.1:p.Thr91Ala | |
| NM_004614.4:c.562A>G | NP_004605.4:p.Thr188Ala | |
| NR_073520.1:n.1841A>G | ||
| NM_001172644.2:c.487A>G | NP_001166115.1:p.Thr163Ala | |
| NM_001271934.2:c.415A>G | NP_001258863.1:p.Thr139Ala | |
| NM_001272050.2:c.271A>G | NP_001258979.1:p.Thr91Ala | |
| NM_004614.5:c.562A>G MANE Select | NP_004605.4:p.Thr188Ala | |
| NR_073520.2:n.1551A>G | ||
| NM_001172645.2:c.508A>G | NP_001166116.1:p.Thr170Ala |