Linked Data
ClinVar Variation Id:
261684
dbSNP Id:
rs1789032
ExAC:
11:77820673 T / C
gnomAD v2:
11-77820673-T-C
gnomAD v3:
11-78109627-T-C
gnomAD v4:
11-78109627-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.78109627T>C , CM000673.2:g.78109627T>C | GRCh38 |
| NC_000011.9:g.77820673T>C , CM000673.1:g.77820673T>C | GRCh37 |
| NC_000011.8:g.77498321T>C | NCBI36 |
| NG_008926.1:g.35027A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299626.10:c.899-46A>G MANE Select | ENSP00000299626.5:n.899-46A>G | |
| ENST00000524925.2:n.1011-46A>G | ||
| ENST00000525761.3:c.635-46A>G | ENSP00000431357.3:n.635-46A>G | |
| ENST00000525783.6:c.635-46A>G | ENSP00000434066.2:n.635-46A>G | |
| ENST00000525870.6:c.899-46A>G | ENSP00000435417.2:n.899-46A>G | |
| ENST00000526737.6:c.*430-46A>G | ENSP00000436366.2:n.*430-46A>G | |
| ENST00000526849.6:c.803-46A>G | ENSP00000434388.2:n.803-46A>G | |
| ENST00000527099.2:c.635-46A>G | ENSP00000436064.2:n.635-46A>G | |
| ENST00000529139.6:c.899-2715A>G | ENSP00000432953.2:n.899-2715A>G | |
| ENST00000530608.6:c.698-46A>G | ENSP00000432381.2:n.698-46A>G | |
| ENST00000530910.6:c.635-46A>G | ENSP00000437033.2:n.635-46A>G | |
| ENST00000532306.6:c.778-2681A>G | ENSP00000435626.2:n.778-2681A>G | |
| ENST00000532440.6:c.899-46A>G | ENSP00000433429.2:n.899-46A>G | |
| ENST00000615266.5:c.899-46A>G | ENSP00000480742.2:n.899-46A>G | |
| ENST00000679444.1:c.635-46A>G | ENSP00000506099.1:n.635-46A>G | |
| ENST00000679497.1:c.635-46A>G | ENSP00000505407.1:n.635-46A>G | |
| ENST00000679539.1:c.899-46A>G | ENSP00000504910.1:n.899-46A>G | |
| ENST00000679559.1:c.899-46A>G | ENSP00000505433.1:n.899-46A>G | |
| ENST00000679581.1:n.1635-46A>G | ||
| ENST00000679648.1:c.*430-46A>G | ENSP00000505726.1:n.*430-46A>G | |
| ENST00000679685.1:c.*283-46A>G | ENSP00000505698.1:n.*283-46A>G | |
| ENST00000679697.1:c.898+3023A>G | ENSP00000505696.1:n.898+3023A>G | |
| ENST00000679874.1:c.*430-46A>G | ENSP00000506314.1:n.*430-46A>G | |
| ENST00000679986.1:c.*430-46A>G | ENSP00000505614.1:n.*430-46A>G | |
| ENST00000680063.1:c.*430-46A>G | ENSP00000504928.1:n.*430-46A>G | |
| ENST00000680101.1:c.635-46A>G | ENSP00000504917.1:n.635-46A>G | |
| ENST00000680142.1:n.905-2715A>G | ||
| ENST00000680223.1:c.899-46A>G | ENSP00000505023.1:n.899-46A>G | |
| ENST00000680256.1:c.902-46A>G | ENSP00000505074.1:n.902-46A>G | |
| ENST00000680329.1:c.635-46A>G | ENSP00000506215.1:n.635-46A>G | |
| ENST00000680398.1:c.899-46A>G | ENSP00000506189.1:n.899-46A>G | |
| ENST00000680399.1:c.899-2715A>G | ENSP00000505984.1:n.899-2715A>G | |
| ENST00000680459.1:c.*522-46A>G | ENSP00000506617.1:n.*522-46A>G | |
| ENST00000680467.1:c.899-2681A>G | ENSP00000505609.1:n.899-2681A>G | |
| ENST00000680499.1:c.635-46A>G | ENSP00000506092.1:n.635-46A>G | |
| ENST00000680580.1:c.635-46A>G | ENSP00000506170.1:n.635-46A>G | |
| ENST00000680643.1:c.899-46A>G | ENSP00000505207.1:n.899-46A>G | |
| ENST00000680761.1:c.635-46A>G | ENSP00000506421.1:n.635-46A>G | |
| ENST00000680797.1:c.*430-46A>G | ENSP00000506717.1:n.*430-46A>G | |
| ENST00000680829.1:c.635-46A>G | ENSP00000506408.1:n.635-46A>G | |
| ENST00000680866.1:c.899-46A>G | ENSP00000505649.1:n.899-46A>G | |
| ENST00000680996.1:c.635-46A>G | ENSP00000505468.1:n.635-46A>G | |
| ENST00000681221.1:c.635-46A>G | ENSP00000505136.1:n.635-46A>G | |
| ENST00000681225.1:c.635-46A>G | ENSP00000505016.1:n.635-46A>G | |
| ENST00000681351.1:c.635-46A>G | ENSP00000506652.1:n.635-46A>G | |
| ENST00000681384.1:c.635-2681A>G | ENSP00000506249.1:n.635-2681A>G | |
| ENST00000681417.1:c.635-46A>G | ENSP00000505965.1:n.635-46A>G | |
| ENST00000681489.1:c.635-46A>G | ENSP00000505200.1:n.635-46A>G | |
| ENST00000681575.1:c.635-46A>G | ENSP00000505743.1:n.635-46A>G | |
| ENST00000681699.1:c.728-46A>G | ENSP00000504969.1:n.728-46A>G | |
| ENST00000681723.1:c.635-46A>G | ENSP00000506059.1:n.635-46A>G | |
| ENST00000681765.1:c.635-2715A>G | ENSP00000505811.1:n.635-2715A>G | |
| ENST00000681853.1:n.1593-46A>G | ||
| ENST00000681957.1:c.899-46A>G | ENSP00000506056.1:n.899-46A>G | |
| ENST00000299626.9:c.899-46A>G | ENSP00000299626.5:n.899-46A>G | |
| ENST00000376156.7:c.899-46A>G | ENSP00000365326.3:n.899-46A>G | |
| ENST00000524925.1:n.337-2681A>G | ||
| ENST00000525783.5:c.103-46A>G | ||
| ENST00000526737.5:c.*531-46A>G | ENSP00000436366.1:n.*531-46A>G | |
| ENST00000530608.5:c.178-2715A>G | ||
| ENST00000532306.5:c.399-2681A>G | ||
| ENST00000532440.5:c.353-46A>G | ENSP00000433429.1:n.353-46A>G | |
| ENST00000532552.2:n.122-46A>G | ||
| ENST00000615266.4:c.899-46A>G | ENSP00000480742.1:n.899-46A>G | |
| NM_001007027.2:c.899-46A>G | NP_001007028.1:n.899-46A>G | |
| NM_024079.4:c.899-46A>G | NP_076984.2:n.899-46A>G | |
| XM_005274247.2:c.872-46A>G | XP_005274304.1:n.872-46A>G | |
| XM_011545251.1:c.899-2715A>G | XP_011543553.1:n.899-2715A>G | |
| XM_011545252.1:c.635-46A>G | XP_011543554.1:n.635-46A>G | |
| XR_428923.2:n.971-46A>G | ||
| XR_950044.1:n.971-46A>G | ||
| XR_950045.1:n.971-46A>G | ||
| XM_005274247.3:c.872-46A>G | XP_005274304.1:n.872-46A>G | |
| XM_011545252.2:c.635-46A>G | XP_011543554.1:n.635-46A>G | |
| XM_017018274.1:c.872-46A>G | XP_016873763.1:n.872-46A>G | |
| XR_001747956.1:n.1721-46A>G | ||
| XR_428923.4:n.954-46A>G | ||
| XR_950044.3:n.954-46A>G | ||
| XR_950045.3:n.954-46A>G | ||
| NM_024079.5:c.899-46A>G MANE Select | NP_076984.2:n.899-46A>G | |
| NM_001007027.3:c.899-46A>G | NP_001007028.1:n.899-46A>G |