Linked Data
ClinVar Variation Id:
2956772
ClinVar RCV Id:
RCV003816483
dbSNP Id:
rs121908294
gnomAD v2:
11-77823770-C-A
gnomAD v3:
11-78112724-C-A
gnomAD v4:
11-78112724-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.78112724C>A , CM000673.2:g.78112724C>A | GRCh38 |
| NC_000011.9:g.77823770C>A , CM000673.1:g.77823770C>A | GRCh37 |
| NC_000011.8:g.77501418C>A | NCBI36 |
| NG_008926.1:g.31930G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299626.10:c.824G>T MANE Select | ENSP00000299626.5:p.Gly275Val | |
| ENST00000524925.2:n.936G>T | ||
| ENST00000525755.6:c.*456G>T | ENSP00000435467.2:n.*456G>T | |
| ENST00000525761.3:c.560G>T | ENSP00000431357.3:p.Gly187Val | |
| ENST00000525783.6:c.560G>T | ENSP00000434066.2:p.Gly187Val | |
| ENST00000525870.6:c.824G>T | ENSP00000435417.2:p.Gly275Val | |
| ENST00000526737.6:c.*355G>T | ENSP00000436366.2:n.*355G>T | |
| ENST00000526849.6:c.728G>T | ENSP00000434388.2:p.Gly243Val | |
| ENST00000527099.2:c.560G>T | ENSP00000436064.2:p.Gly187Val | |
| ENST00000529139.6:c.824G>T | ENSP00000432953.2:p.Gly275Val | |
| ENST00000530454.6:c.824G>T | ENSP00000434660.2:p.Gly275Val | |
| ENST00000530608.6:c.623G>T | ENSP00000432381.2:p.Gly208Val | |
| ENST00000530910.6:c.560G>T | ENSP00000437033.2:p.Gly187Val | |
| ENST00000532306.6:c.777+1162G>T | ENSP00000435626.2:n.777+1162G>T | |
| ENST00000532440.6:c.824G>T | ENSP00000433429.2:p.Gly275Val | |
| ENST00000615266.5:c.824G>T | ENSP00000480742.2:p.Gly275Val | |
| ENST00000679444.1:c.560G>T | ENSP00000506099.1:p.Gly187Val | |
| ENST00000679497.1:c.560G>T | ENSP00000505407.1:p.Gly187Val | |
| ENST00000679539.1:c.824G>T | ENSP00000504910.1:p.Gly275Val | |
| ENST00000679559.1:c.824G>T | ENSP00000505433.1:p.Gly275Val | |
| ENST00000679581.1:n.1560G>T | ||
| ENST00000679648.1:c.*355G>T | ENSP00000505726.1:n.*355G>T | |
| ENST00000679685.1:c.*208G>T | ENSP00000505698.1:n.*208G>T | |
| ENST00000679697.1:c.824G>T | ENSP00000505696.1:p.Gly275Val | |
| ENST00000679874.1:c.*355G>T | ENSP00000506314.1:n.*355G>T | |
| ENST00000679986.1:c.*355G>T | ENSP00000505614.1:n.*355G>T | |
| ENST00000680063.1:c.*355G>T | ENSP00000504928.1:n.*355G>T | |
| ENST00000680101.1:c.560G>T | ENSP00000504917.1:p.Gly187Val | |
| ENST00000680142.1:n.905-5812G>T | ||
| ENST00000680223.1:c.824G>T | ENSP00000505023.1:p.Gly275Val | |
| ENST00000680256.1:c.827G>T | ENSP00000505074.1:p.Gly276Val | |
| ENST00000680329.1:c.560G>T | ENSP00000506215.1:p.Gly187Val | |
| ENST00000680398.1:c.824G>T | ENSP00000506189.1:p.Gly275Val | |
| ENST00000680399.1:c.824G>T | ENSP00000505984.1:p.Gly275Val | |
| ENST00000680459.1:c.*447G>T | ENSP00000506617.1:n.*447G>T | |
| ENST00000680467.1:c.824G>T | ENSP00000505609.1:p.Gly275Val | |
| ENST00000680499.1:c.560G>T | ENSP00000506092.1:p.Gly187Val | |
| ENST00000680580.1:c.560G>T | ENSP00000506170.1:p.Gly187Val | |
| ENST00000680643.1:c.824G>T | ENSP00000505207.1:p.Gly275Val | |
| ENST00000680761.1:c.560G>T | ENSP00000506421.1:p.Gly187Val | |
| ENST00000680797.1:c.*355G>T | ENSP00000506717.1:n.*355G>T | |
| ENST00000680829.1:c.560G>T | ENSP00000506408.1:p.Gly187Val | |
| ENST00000680866.1:c.824G>T | ENSP00000505649.1:p.Gly275Val | |
| ENST00000680996.1:c.560G>T | ENSP00000505468.1:p.Gly187Val | |
| ENST00000681221.1:c.560G>T | ENSP00000505136.1:p.Gly187Val | |
| ENST00000681225.1:c.560G>T | ENSP00000505016.1:p.Gly187Val | |
| ENST00000681351.1:c.560G>T | ENSP00000506652.1:p.Gly187Val | |
| ENST00000681384.1:c.560G>T | ENSP00000506249.1:p.Gly187Val | |
| ENST00000681417.1:c.560G>T | ENSP00000505965.1:p.Gly187Val | |
| ENST00000681489.1:c.560G>T | ENSP00000505200.1:p.Gly187Val | |
| ENST00000681575.1:c.560G>T | ENSP00000505743.1:p.Gly187Val | |
| ENST00000681699.1:c.653G>T | ENSP00000504969.1:p.Gly218Val | |
| ENST00000681723.1:c.560G>T | ENSP00000506059.1:p.Gly187Val | |
| ENST00000681765.1:c.560G>T | ENSP00000505811.1:p.Gly187Val | |
| ENST00000681853.1:n.1518G>T | ||
| ENST00000681957.1:c.824G>T | ENSP00000506056.1:p.Gly275Val | |
| ENST00000299626.9:c.824G>T | ENSP00000299626.5:p.Gly275Val | |
| ENST00000376156.7:c.824G>T | ENSP00000365326.3:p.Gly275Val | |
| ENST00000524925.1:n.262G>T | ||
| ENST00000525755.5:c.671G>T | ENSP00000435467.1:p.Gly224Val | |
| ENST00000525783.5:c.28G>T | ||
| ENST00000526737.5:c.*456G>T | ENSP00000436366.1:n.*456G>T | |
| ENST00000529139.5:c.358G>T | ||
| ENST00000530454.5:c.827G>T | ENSP00000434660.1:p.Gly276Val | |
| ENST00000530608.5:c.103G>T | ||
| ENST00000532306.5:c.398+1162G>T | ||
| ENST00000532440.5:c.278G>T | ENSP00000433429.1:p.Gly93Val | |
| ENST00000532552.2:n.122-3143G>T | ||
| ENST00000615266.4:c.824G>T | ENSP00000480742.1:p.Gly275Val | |
| NM_001007027.2:c.824G>T | NP_001007028.1:p.Gly275Val | |
| NM_024079.4:c.824G>T | NP_076984.2:p.Gly275Val | |
| XM_005274247.2:c.797G>T | XP_005274304.1:p.Gly266Val | |
| XM_011545251.1:c.824G>T | XP_011543553.1:p.Gly275Val | |
| XM_011545252.1:c.560G>T | XP_011543554.1:p.Gly187Val | |
| XR_428923.2:n.896G>T | ||
| XR_950044.1:n.896G>T | ||
| XR_950045.1:n.896G>T | ||
| XM_005274247.3:c.797G>T | XP_005274304.1:p.Gly266Val | |
| XM_011545252.2:c.560G>T | XP_011543554.1:p.Gly187Val | |
| XM_017018274.1:c.797G>T | XP_016873763.1:p.Gly266Val | |
| XR_001747956.1:n.1646G>T | ||
| XR_428923.4:n.879G>T | ||
| XR_950044.3:n.879G>T | ||
| XR_950045.3:n.879G>T | ||
| NM_024079.5:c.824G>T MANE Select | NP_076984.2:p.Gly275Val | |
| NM_001007027.3:c.824G>T | NP_001007028.1:p.Gly275Val |