Linked Data
ClinVar Variation Id:
1146436
ClinVar RCV Id:
RCV001485673
dbSNP Id:
rs780518207
ExAC:
20:43252921 G / C
gnomAD v2:
20-43252921-G-C
gnomAD v4:
20-44624280-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44624280G>C , CM000682.2:g.44624280G>C | GRCh38 |
| NC_000020.10:g.43252921G>C , CM000682.1:g.43252921G>C | GRCh37 |
| NC_000020.9:g.42686335G>C | NCBI36 |
| NG_007385.1:g.32456C>G , LRG_16:g.32456C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000492931.6:n.619C>G | ||
| ENST00000536076.2:c.375C>G | ENSP00000512234.1:p.Thr125= | |
| ENST00000536532.6:c.528C>G | ENSP00000440946.1:p.Thr176= | |
| ENST00000537820.2:c.528C>G | ENSP00000441818.1:p.Thr176= | |
| ENST00000539235.6:c.219-1202C>G | ENSP00000446464.1:n.219-1202C>G | |
| ENST00000695889.1:c.219-1350C>G | ENSP00000512240.1:n.219-1350C>G | |
| ENST00000695890.1:n.2331C>G | ||
| ENST00000695891.1:c.219-1350C>G | ENSP00000512241.1:n.219-1350C>G | |
| ENST00000695927.1:c.606C>G | ENSP00000512270.1:p.Thr202= | |
| ENST00000695949.1:c.525C>G | ENSP00000512281.1:p.Thr175= | |
| ENST00000695957.1:c.*19C>G | ENSP00000512286.1:n.*19C>G | |
| ENST00000695991.1:c.217-1350C>G | ENSP00000512314.1:n.217-1350C>G | |
| ENST00000695992.1:c.528C>G | ENSP00000512315.1:p.Thr176= | |
| ENST00000695993.1:c.528C>G | ENSP00000512316.1:p.Thr176= | |
| ENST00000695994.1:c.528C>G | ENSP00000512317.1:p.Thr176= | |
| ENST00000695995.1:c.217-1202C>G | ENSP00000512318.1:n.217-1202C>G | |
| ENST00000695996.1:n.599C>G | ||
| ENST00000695997.1:n.483C>G | ||
| ENST00000696003.1:n.620C>G | ||
| ENST00000696004.1:n.620C>G | ||
| ENST00000696005.1:c.50C>G | ||
| ENST00000696006.1:c.528C>G | ENSP00000512325.1:p.Thr176= | |
| ENST00000696007.1:c.379C>G | ENSP00000512326.1:n.379C>G | |
| ENST00000696008.1:n.1683C>G | ||
| ENST00000696009.1:n.1878C>G | ||
| ENST00000696017.1:c.525C>G | ENSP00000512333.1:p.Thr175= | |
| ENST00000696034.1:c.528C>G | ENSP00000512343.1:p.Thr176= | |
| ENST00000696035.1:n.638C>G | ||
| ENST00000696036.1:n.1218C>G | ||
| ENST00000696037.1:n.2205C>G | ||
| ENST00000696038.1:c.*274C>G | ENSP00000512344.1:n.*274C>G | |
| ENST00000696039.1:n.816C>G | ||
| ENST00000696058.1:c.528C>G | ENSP00000512361.1:p.Thr176= | |
| ENST00000696059.1:c.*473C>G | ENSP00000512362.1:n.*473C>G | |
| ENST00000696060.1:c.528C>G | ENSP00000512363.1:p.Thr176= | |
| ENST00000696061.1:c.525C>G | ENSP00000512364.1:p.Thr175= | |
| ENST00000696062.1:c.591C>G | ENSP00000512365.1:p.Thr197= | |
| ENST00000696063.1:c.603C>G | ENSP00000512366.1:p.Thr201= | |
| ENST00000696064.1:c.375C>G | ENSP00000512367.1:p.Thr125= | |
| ENST00000696065.1:c.66-1350C>G | ENSP00000512368.1:n.66-1350C>G | |
| ENST00000696074.1:n.144C>G | ||
| ENST00000696075.1:c.*498C>G | ENSP00000512374.1:n.*498C>G | |
| ENST00000696076.1:c.528C>G | ENSP00000512375.1:p.Thr176= | |
| ENST00000696077.1:c.525C>G | ENSP00000512376.1:p.Thr175= | |
| ENST00000696078.1:c.528C>G | ENSP00000512377.1:p.Thr176= | |
| ENST00000696079.1:c.528C>G | ENSP00000512378.1:p.Thr176= | |
| ENST00000696080.1:c.528C>G | ENSP00000512379.1:p.Thr176= | |
| ENST00000696081.1:n.647C>G | ||
| ENST00000696082.1:c.606C>G | ENSP00000512380.1:p.Thr202= | |
| ENST00000696083.1:n.1409C>G | ||
| ENST00000696084.1:n.629C>G | ||
| ENST00000696104.1:c.363-1350C>G | ENSP00000512399.1:n.363-1350C>G | |
| ENST00000696105.1:c.*69C>G | ENSP00000512400.1:n.*69C>G | |
| ENST00000372874.9:c.528C>G MANE Select | ENSP00000361965.4:p.Thr176= | |
| ENST00000372874.8:c.528C>G | ENSP00000361965.4:p.Thr176= | |
| ENST00000464097.5:n.202C>G | ||
| ENST00000492931.5:n.612C>G | ||
| ENST00000536532.5:c.528C>G | ENSP00000440946.1:p.Thr176= | |
| ENST00000537820.1:c.528C>G | ENSP00000441818.1:p.Thr176= | |
| ENST00000539235.5:c.219-1202C>G | ENSP00000446464.1:n.219-1202C>G | |
| NM_000022.2:c.528C>G , LRG_16t1:c.528C>G | NP_000013.2:p.Thr176= | |
| XM_005260236.2:c.528C>G | XP_005260293.1:p.Thr176= | |
| XM_011528478.1:c.123C>G | XP_011526780.1:p.Thr41= | |
| XM_011528479.1:c.123C>G | XP_011526781.1:p.Thr41= | |
| XR_244129.1:n.582C>G | ||
| NM_000022.3:c.528C>G | NP_000013.2:p.Thr176= | |
| NM_001322050.1:c.123C>G | NP_001308979.1:p.Thr41= | |
| NM_001322051.1:c.528C>G | NP_001308980.1:p.Thr176= | |
| NR_136160.1:n.679C>G | ||
| NM_000022.4:c.528C>G MANE Select | NP_000013.2:p.Thr176= | |
| NM_001322050.2:c.123C>G | NP_001308979.1:p.Thr41= | |
| NM_001322051.2:c.528C>G | NP_001308980.1:p.Thr176= | |
| NR_136160.2:n.620C>G |