MyVariant.info:
GRCh37
chr11:g.17436136A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17414589A>G , CM000673.2:g.17414589A>G | GRCh38 |
| NC_000011.9:g.17436136A>G , CM000673.1:g.17436136A>G | GRCh37 |
| NC_000011.8:g.17392712A>G | NCBI36 |
| NG_008867.1:g.67314T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524561.2:n.1982T>C | ||
| ENST00000529967.6:n.572T>C | ||
| ENST00000642611.2:n.2382T>C | ||
| ENST00000682051.1:n.2329T>C | ||
| ENST00000682110.1:n.2382T>C | ||
| ENST00000682140.1:c.2310T>C | ENSP00000507829.1:p.Tyr770= | |
| ENST00000682185.1:n.3618T>C | ||
| ENST00000682204.1:c.*451T>C | ENSP00000507094.1:n.*451T>C | |
| ENST00000682215.1:n.2379T>C | ||
| ENST00000682288.1:c.*744T>C | ENSP00000507506.1:n.*744T>C | |
| ENST00000682442.1:n.2503T>C | ||
| ENST00000682528.1:n.2379T>C | ||
| ENST00000682673.1:n.2326T>C | ||
| ENST00000682805.1:n.2379T>C | ||
| ENST00000682965.1:c.2310T>C | ENSP00000508229.1:p.Tyr770= | |
| ENST00000683093.1:n.2481T>C | ||
| ENST00000683136.1:c.2310T>C | ENSP00000507768.1:p.Tyr770= | |
| ENST00000683153.1:n.2538T>C | ||
| ENST00000683365.1:n.2484T>C | ||
| ENST00000683377.1:n.2382T>C | ||
| ENST00000683456.1:c.2313T>C | ENSP00000508318.1:p.Tyr771= | |
| ENST00000683522.1:n.2382T>C | ||
| ENST00000683562.1:c.*482T>C | ENSP00000508265.1:n.*482T>C | |
| ENST00000683693.1:n.2379T>C | ||
| ENST00000683725.1:c.2313T>C | ENSP00000507496.1:p.Tyr771= | |
| ENST00000684010.1:n.2382T>C | ||
| ENST00000684157.1:n.2382T>C | ||
| ENST00000684253.1:n.2285T>C | ||
| ENST00000684288.1:c.*485T>C | ENSP00000507143.1:n.*485T>C | |
| ENST00000684313.1:n.1814T>C | ||
| ENST00000684332.1:n.2455T>C | ||
| ENST00000684371.1:n.2488T>C | ||
| ENST00000684404.1:n.2379T>C | ||
| ENST00000684442.1:n.2382T>C | ||
| ENST00000684555.1:c.*525T>C | ENSP00000507705.1:n.*525T>C | |
| ENST00000684571.1:c.2154T>C | ENSP00000506935.1:p.Tyr718= | |
| ENST00000684593.1:c.*2018T>C | ENSP00000507005.1:n.*2018T>C | |
| ENST00000684711.1:c.*709T>C | ENSP00000506841.1:n.*709T>C | |
| ENST00000302539.9:c.2316T>C | ENSP00000303960.4:p.Tyr772= | |
| ENST00000389817.8:c.2313T>C MANE Select | ENSP00000374467.4:p.Tyr771= | |
| ENST00000642271.1:c.2310T>C | ENSP00000493749.1:p.Tyr770= | |
| ENST00000642579.1:c.397T>C | ||
| ENST00000642611.1:n.2267T>C | ||
| ENST00000642902.1:c.2148T>C | ||
| ENST00000643260.1:c.2313T>C | ENSP00000494450.1:p.Tyr771= | |
| ENST00000643562.1:c.*289T>C | ENSP00000496124.1:n.*289T>C | |
| ENST00000643925.1:c.253T>C | ||
| ENST00000644447.1:c.669T>C | ENSP00000496282.1:p.Tyr223= | |
| ENST00000644472.1:c.*674T>C | ENSP00000495378.1:n.*674T>C | |
| ENST00000644484.1:c.*522T>C | ENSP00000493558.1:n.*522T>C | |
| ENST00000644542.1:c.*2018T>C | ENSP00000495532.1:n.*2018T>C | |
| ENST00000644675.1:c.*485T>C | ENSP00000494567.1:n.*485T>C | |
| ENST00000644757.1:c.*618T>C | ENSP00000495085.1:n.*618T>C | |
| ENST00000644772.1:c.2379T>C | ENSP00000494321.1:p.Tyr793= | |
| ENST00000645076.1:c.1565T>C | ||
| ENST00000645744.1:c.*677T>C | ENSP00000494564.1:n.*677T>C | |
| ENST00000645760.1:c.2588T>C | ||
| ENST00000645884.1:c.2313T>C | ENSP00000495516.1:p.Tyr771= | |
| ENST00000646003.1:c.*454T>C | ENSP00000495259.1:n.*454T>C | |
| ENST00000646207.1:c.*677T>C | ENSP00000495025.1:n.*677T>C | |
| ENST00000646276.1:c.*586T>C | ENSP00000496070.1:n.*586T>C | |
| ENST00000646592.1:c.1539T>C | ||
| ENST00000646902.1:c.2310T>C | ENSP00000494101.1:p.Tyr770= | |
| ENST00000646993.1:c.*709T>C | ENSP00000493720.1:n.*709T>C | |
| ENST00000647013.1:c.2319T>C | ENSP00000496741.1:n.2319T>C | |
| ENST00000647015.1:c.2064T>C | ENSP00000495389.1:p.Tyr688= | |
| ENST00000647086.1:c.*2043T>C | ENSP00000493677.1:n.*2043T>C | |
| ENST00000647158.1:c.*454T>C | ENSP00000495744.1:n.*454T>C | |
| ENST00000302539.8:c.2316T>C | ENSP00000303960.4:p.Tyr772= | |
| ENST00000389817.7:c.2313T>C | ENSP00000374467.3:p.Tyr771= | |
| ENST00000527905.5:c.2283T>C | ENSP00000431653.1:p.Tyr761= | |
| ENST00000531911.1:n.427T>C | ||
| NM_000352.4:c.2313T>C | NP_000343.2:p.Tyr771= | |
| NM_001287174.1:c.2316T>C | NP_001274103.1:p.Tyr772= | |
| XM_011520331.1:c.2313T>C | XP_011518633.1:p.Tyr771= | |
| XM_011520332.1:c.2316T>C | XP_011518634.1:p.Tyr772= | |
| XM_011520333.1:c.813T>C | XP_011518635.1:p.Tyr271= | |
| XM_011520334.1:c.2316T>C | XP_011518636.1:p.Tyr772= | |
| XR_930890.1:n.2379T>C | ||
| XR_930891.1:n.2379T>C | ||
| XR_930892.1:n.2379T>C | ||
| XR_930893.1:n.2376T>C | ||
| NM_001351295.1:c.2379T>C | NP_001338224.1:p.Tyr793= | |
| NM_001351296.1:c.2313T>C | NP_001338225.1:p.Tyr771= | |
| NM_001351297.1:c.2310T>C | NP_001338226.1:p.Tyr770= | |
| NR_147094.1:n.2382T>C | ||
| XM_017018197.2:c.2382T>C | XP_016873686.1:p.Tyr794= | |
| XM_017018199.1:c.2379T>C | XP_016873688.1:p.Tyr793= | |
| XM_017018201.2:c.2382T>C | XP_016873690.1:p.Tyr794= | |
| XM_017018202.1:c.879T>C | XP_016873691.1:p.Tyr293= | |
| XM_017018204.1:c.270T>C | XP_016873693.1:p.Tyr90= | |
| XM_024448668.1:c.681T>C | XP_024304436.1:p.Tyr227= | |
| XR_001747945.2:n.2454T>C | ||
| XR_001747946.2:n.2385T>C | ||
| XR_002957189.1:n.2454T>C | ||
| NM_000352.6:c.2313T>C MANE Select | NP_000343.2:p.Tyr771= | |
| NM_001287174.2:c.2316T>C | NP_001274103.1:p.Tyr772= | |
| NM_001351295.2:c.2379T>C | NP_001338224.1:p.Tyr793= | |
| NM_001351296.2:c.2313T>C | NP_001338225.1:p.Tyr771= | |
| NM_001351297.2:c.2310T>C | NP_001338226.1:p.Tyr770= | |
| NR_147094.2:n.2382T>C | ||
| NM_001287174.3:c.2316T>C | NP_001274103.1:p.Tyr772= |