Linked Data
ClinVar Variation Id:
753254
dbSNP Id:
rs371724951
gnomAD v3:
11-17428307-A-G
gnomAD v4:
11-17428307-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17428307A>G , CM000673.2:g.17428307A>G | GRCh38 |
| NC_000011.9:g.17449854A>G , CM000673.1:g.17449854A>G | GRCh37 |
| NC_000011.8:g.17406430A>G | NCBI36 |
| NG_008867.1:g.53596T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524561.2:n.1691T>C | ||
| ENST00000529967.6:n.281T>C | ||
| ENST00000642611.2:n.2088T>C | ||
| ENST00000682051.1:n.2035T>C | ||
| ENST00000682110.1:n.2088T>C | ||
| ENST00000682140.1:c.2019T>C | ENSP00000507829.1:p.Ala673= | |
| ENST00000682185.1:n.3327T>C | ||
| ENST00000682204.1:c.*160T>C | ENSP00000507094.1:n.*160T>C | |
| ENST00000682215.1:n.2088T>C | ||
| ENST00000682288.1:c.*450T>C | ENSP00000507506.1:n.*450T>C | |
| ENST00000682442.1:n.2209T>C | ||
| ENST00000682528.1:n.2088T>C | ||
| ENST00000682673.1:n.2035T>C | ||
| ENST00000682805.1:n.2088T>C | ||
| ENST00000682965.1:c.2019T>C | ENSP00000508229.1:p.Ala673= | |
| ENST00000683093.1:n.2190T>C | ||
| ENST00000683136.1:c.2019T>C | ENSP00000507768.1:p.Ala673= | |
| ENST00000683153.1:n.2247T>C | ||
| ENST00000683253.1:n.3104T>C | ||
| ENST00000683365.1:n.2190T>C | ||
| ENST00000683377.1:n.2088T>C | ||
| ENST00000683456.1:c.2019T>C | ENSP00000508318.1:p.Ala673= | |
| ENST00000683522.1:n.2088T>C | ||
| ENST00000683562.1:c.*191T>C | ENSP00000508265.1:n.*191T>C | |
| ENST00000683693.1:n.2088T>C | ||
| ENST00000683725.1:c.2022T>C | ENSP00000507496.1:p.Ala674= | |
| ENST00000684010.1:n.2088T>C | ||
| ENST00000684157.1:n.2088T>C | ||
| ENST00000684253.1:n.1994T>C | ||
| ENST00000684288.1:c.*191T>C | ENSP00000507143.1:n.*191T>C | |
| ENST00000684313.1:n.1724-11345T>C | ||
| ENST00000684332.1:n.2161T>C | ||
| ENST00000684371.1:n.2194T>C | ||
| ENST00000684404.1:n.2088T>C | ||
| ENST00000684442.1:n.2088T>C | ||
| ENST00000684555.1:c.*231T>C | ENSP00000507705.1:n.*231T>C | |
| ENST00000684571.1:c.1863T>C | ENSP00000506935.1:p.Ala621= | |
| ENST00000684593.1:c.*1727T>C | ENSP00000507005.1:n.*1727T>C | |
| ENST00000684711.1:c.*418T>C | ENSP00000506841.1:n.*418T>C | |
| ENST00000302539.9:c.2022T>C | ENSP00000303960.4:p.Ala674= | |
| ENST00000389817.8:c.2022T>C MANE Select | ENSP00000374467.4:p.Ala674= | |
| ENST00000532728.6:c.1603T>C | ||
| ENST00000642271.1:c.2019T>C | ENSP00000493749.1:p.Ala673= | |
| ENST00000642579.1:c.103T>C | ||
| ENST00000642611.1:n.1973T>C | ||
| ENST00000642902.1:c.1857T>C | ||
| ENST00000643260.1:c.2019T>C | ENSP00000494450.1:p.Ala673= | |
| ENST00000643562.1:c.2014T>C | ENSP00000496124.1:p.Ter672Arg | |
| ENST00000644447.1:c.375T>C | ENSP00000496282.1:p.Ala125= | |
| ENST00000644472.1:c.*383T>C | ENSP00000495378.1:n.*383T>C | |
| ENST00000644484.1:c.*231T>C | ENSP00000493558.1:n.*231T>C | |
| ENST00000644542.1:c.*1724T>C | ENSP00000495532.1:n.*1724T>C | |
| ENST00000644649.1:c.1192T>C | ||
| ENST00000644675.1:c.*191T>C | ENSP00000494567.1:n.*191T>C | |
| ENST00000644757.1:c.*324T>C | ENSP00000495085.1:n.*324T>C | |
| ENST00000644772.1:c.2088T>C | ENSP00000494321.1:p.Ala696= | |
| ENST00000645076.1:c.1274T>C | ||
| ENST00000645744.1:c.*383T>C | ENSP00000494564.1:n.*383T>C | |
| ENST00000645760.1:c.2297T>C | ||
| ENST00000645884.1:c.2019T>C | ENSP00000495516.1:p.Ala673= | |
| ENST00000646003.1:c.*160T>C | ENSP00000495259.1:n.*160T>C | |
| ENST00000646207.1:c.*383T>C | ENSP00000495025.1:n.*383T>C | |
| ENST00000646276.1:c.*292T>C | ENSP00000496070.1:n.*292T>C | |
| ENST00000646592.1:c.1245T>C | ||
| ENST00000646902.1:c.2019T>C | ENSP00000494101.1:p.Ala673= | |
| ENST00000646993.1:c.*418T>C | ENSP00000493720.1:n.*418T>C | |
| ENST00000647013.1:c.2025T>C | ENSP00000496741.1:n.2025T>C | |
| ENST00000647015.1:c.1770T>C | ENSP00000495389.1:p.Ala590= | |
| ENST00000647086.1:c.*1749T>C | ENSP00000493677.1:n.*1749T>C | |
| ENST00000647158.1:c.*160T>C | ENSP00000495744.1:n.*160T>C | |
| ENST00000302539.8:c.2022T>C | ENSP00000303960.4:p.Ala674= | |
| ENST00000389817.7:c.2022T>C | ENSP00000374467.3:p.Ala674= | |
| ENST00000527905.5:c.1992T>C | ENSP00000431653.1:p.Ala664= | |
| NM_000352.4:c.2022T>C | NP_000343.2:p.Ala674= | |
| NM_001287174.1:c.2022T>C | NP_001274103.1:p.Ala674= | |
| XM_011520331.1:c.2019T>C | XP_011518633.1:p.Ala673= | |
| XM_011520332.1:c.2022T>C | XP_011518634.1:p.Ala674= | |
| XM_011520333.1:c.519T>C | XP_011518635.1:p.Ala173= | |
| XM_011520334.1:c.2022T>C | XP_011518636.1:p.Ala674= | |
| XR_930890.1:n.2085T>C | ||
| XR_930891.1:n.2085T>C | ||
| XR_930892.1:n.2085T>C | ||
| XR_930893.1:n.2085T>C | ||
| NM_001351295.1:c.2088T>C | NP_001338224.1:p.Ala696= | |
| NM_001351296.1:c.2019T>C | NP_001338225.1:p.Ala673= | |
| NM_001351297.1:c.2019T>C | NP_001338226.1:p.Ala673= | |
| NR_147094.1:n.2088T>C | ||
| XM_017018197.2:c.2088T>C | XP_016873686.1:p.Ala696= | |
| XM_017018199.1:c.2085T>C | XP_016873688.1:p.Ala695= | |
| XM_017018201.2:c.2088T>C | XP_016873690.1:p.Ala696= | |
| XM_017018202.1:c.585T>C | XP_016873691.1:p.Ala195= | |
| XM_017018204.1:c.-22T>C | XP_016873693.1:n.-22T>C | |
| XM_024448668.1:c.387T>C | XP_024304436.1:p.Ala129= | |
| XR_001747945.2:n.2160T>C | ||
| XR_001747946.2:n.2094T>C | ||
| XR_002957189.1:n.2160T>C | ||
| NM_000352.6:c.2022T>C MANE Select | NP_000343.2:p.Ala674= | |
| NM_001287174.2:c.2022T>C | NP_001274103.1:p.Ala674= | |
| NM_001351295.2:c.2088T>C | NP_001338224.1:p.Ala696= | |
| NM_001351296.2:c.2019T>C | NP_001338225.1:p.Ala673= | |
| NM_001351297.2:c.2019T>C | NP_001338226.1:p.Ala673= | |
| NR_147094.2:n.2088T>C | ||
| NM_001287174.3:c.2022T>C | NP_001274103.1:p.Ala674= |