Linked Data
dbSNP Id:
rs1365374040
gnomAD v2:
2-202141616-A-G
gnomAD v3:
2-201276893-A-G
gnomAD v4:
2-201276893-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.201276893A>G , CM000664.2:g.201276893A>G | GRCh38 |
| NC_000002.11:g.202141616A>G , CM000664.1:g.202141616A>G | GRCh37 |
| NC_000002.10:g.201849861A>G | NCBI36 |
| NG_007497.1:g.48436A>G , LRG_34:g.48436A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413726.6:c.727A>G | ENSP00000397528.2:p.Asn243Asp | |
| ENST00000440732.6:c.727A>G | ENSP00000396869.2:p.Asn243Asp | |
| ENST00000444430.3:c.550+4117A>G | ENSP00000394434.3:n.550+4117A>G | |
| ENST00000447616.6:c.617A>G | ENSP00000388306.2:p.Gln206Arg | |
| ENST00000450491.6:c.373A>G | ENSP00000391709.2:p.Asn125Asp | |
| ENST00000696067.1:c.727A>G | ENSP00000512369.1:p.Asn243Asp | |
| ENST00000696068.1:c.617A>G | ENSP00000512370.1:p.Gln206Arg | |
| ENST00000696069.1:c.682A>G | ENSP00000512371.1:p.Asn228Asp | |
| ENST00000696085.1:c.859A>G | ENSP00000512381.1:p.Asn287Asp | |
| ENST00000696087.1:c.682A>G | ENSP00000512382.1:p.Asn228Asp | |
| ENST00000673742.1:c.727A>G MANE Select | ENSP00000501268.1:p.Asn243Asp | |
| ENST00000264274.13:c.550+4117A>G | ENSP00000264274.9:n.550+4117A>G | |
| ENST00000264275.9:c.778A>G | ENSP00000264275.5:p.Asn260Asp | |
| ENST00000323492.11:c.682A>G | ENSP00000325722.7:p.Asn228Asp | |
| ENST00000339403.6:n.812A>G | ||
| ENST00000358485.8:c.904A>G | ENSP00000351273.4:p.Asn302Asp | |
| ENST00000392258.7:c.662A>G | ENSP00000376087.3:p.Gln221Arg | |
| ENST00000392263.6:c.682A>G | ENSP00000376091.2:p.Asn228Asp | |
| ENST00000392266.7:c.682A>G | ENSP00000376094.4:p.Asn228Asp | |
| ENST00000424461.5:c.206A>G | ENSP00000390346.1:p.Gln69Arg | |
| ENST00000432109.6:c.727A>G | ENSP00000412523.2:p.Asn243Asp | |
| ENST00000444430.2:c.139+4117A>G | ENSP00000394434.2:n.139+4117A>G | |
| ENST00000447616.5:c.617A>G | ENSP00000388306.1:p.Gln206Arg | |
| ENST00000450491.5:c.373A>G | ENSP00000391709.1:p.Asn125Asp | |
| NM_001080124.1:c.682A>G | NP_001073593.1:p.Asn228Asp | |
| NM_001080125.1:c.904A>G | NP_001073594.1:p.Asn302Asp | |
| NM_001228.4:c.778A>G , LRG_34t1:c.778A>G | NP_001219.2:p.Asn260Asp | |
| NM_033355.3:c.727A>G , LRG_34t2:c.727A>G | NP_203519.1:p.Asn243Asp | |
| NM_033356.3:c.682A>G | NP_203520.1:p.Asn228Asp | |
| NM_033358.3:c.662A>G | NP_203522.1:p.Gln221Arg | |
| NR_111983.1:n.1105A>G | ||
| XM_005246885.1:c.859A>G | XP_005246942.1:p.Asn287Asp | |
| XM_005246886.1:c.727A>G | XP_005246943.1:p.Asn243Asp | |
| XM_005246887.1:c.727A>G | XP_005246944.1:p.Asn243Asp | |
| XM_005246888.1:c.727A>G | XP_005246945.1:p.Asn243Asp | |
| XM_005246889.1:c.727A>G | XP_005246946.1:p.Asn243Asp | |
| XM_005246890.2:c.727A>G | XP_005246947.1:p.Asn243Asp | |
| XM_005246891.3:c.727A>G | XP_005246948.1:p.Asn243Asp | |
| XM_005246892.1:c.682A>G | XP_005246949.1:p.Asn228Asp | |
| XM_005246893.2:c.839A>G | XP_005246950.1:p.Gln280Arg | |
| XM_005246894.2:c.130A>G | XP_005246951.1:p.Asn44Asp | |
| XM_005246895.2:c.794A>G | XP_005246952.1:p.Gln265Arg | |
| XM_006712789.1:c.727A>G | XP_006712852.1:p.Asn243Asp | |
| XM_006712790.2:c.727A>G | XP_006712853.1:p.Asn243Asp | |
| XM_006712791.1:c.727+4117A>G | XP_006712854.1:n.727+4117A>G | |
| XM_006712793.2:c.662A>G | XP_006712856.1:p.Gln221Arg | |
| XM_011511968.1:c.904A>G | XP_011510270.1:p.Asn302Asp | |
| XM_011511969.1:c.292A>G | XP_011510271.1:p.Asn98Asp | |
| XM_011511970.1:c.839A>G | XP_011510272.1:p.Gln280Arg | |
| XR_923035.1:n.860A>G | ||
| XM_005246885.2:c.859A>G | XP_005246942.1:p.Asn287Asp | |
| XM_005246886.2:c.727A>G | XP_005246943.1:p.Asn243Asp | |
| XM_005246887.2:c.727A>G | XP_005246944.1:p.Asn243Asp | |
| XM_005246888.2:c.727A>G | XP_005246945.1:p.Asn243Asp | |
| XM_005246889.2:c.727A>G | XP_005246946.1:p.Asn243Asp | |
| XM_005246890.4:c.727A>G | XP_005246947.1:p.Asn243Asp | |
| XM_005246891.5:c.727A>G | XP_005246948.1:p.Asn243Asp | |
| XM_005246892.2:c.682A>G | XP_005246949.1:p.Asn228Asp | |
| XM_005246893.3:c.839A>G | XP_005246950.1:p.Gln280Arg | |
| XM_005246894.4:c.130A>G | XP_005246951.1:p.Asn44Asp | |
| XM_005246895.3:c.794A>G | XP_005246952.1:p.Gln265Arg | |
| XM_006712789.2:c.727A>G | XP_006712852.1:p.Asn243Asp | |
| XM_006712790.4:c.727A>G | XP_006712853.1:p.Asn243Asp | |
| XM_006712793.3:c.662A>G | XP_006712856.1:p.Gln221Arg | |
| XM_011511969.2:c.292A>G | XP_011510271.1:p.Asn98Asp | |
| XR_001738971.1:n.938A>G | ||
| NM_001080124.2:c.682A>G | NP_001073593.1:p.Asn228Asp | |
| NM_001080125.2:c.904A>G | NP_001073594.1:p.Asn302Asp | |
| NM_001372051.1:c.727A>G MANE Select | NP_001358980.1:p.Asn243Asp | |
| NM_033356.4:c.682A>G | NP_203520.1:p.Asn228Asp | |
| NM_033358.4:c.662A>G | NP_203522.1:p.Gln221Arg | |
| NR_111983.2:n.1101A>G | ||
| NM_001400642.1:c.859A>G | NP_001387571.1:p.Asn287Asp | |
| NM_001400645.1:c.760A>G | NP_001387574.1:p.Asn254Asp | |
| NM_001400648.1:c.727A>G | NP_001387577.1:p.Asn243Asp | |
| NM_001400651.1:c.727A>G | NP_001387580.1:p.Asn243Asp | |
| NM_001400653.1:c.727A>G | NP_001387582.1:p.Asn243Asp | |
| NM_001400654.1:c.727A>G | NP_001387583.1:p.Asn243Asp | |
| NM_001400655.1:c.727A>G | NP_001387584.1:p.Asn243Asp | |
| NM_001400656.1:c.727A>G | NP_001387585.1:p.Asn243Asp | |
| NM_001400657.1:c.727A>G | NP_001387586.1:p.Asn243Asp | |
| NM_001400658.1:c.682A>G | NP_001387587.1:p.Asn228Asp | |
| NM_001400659.1:c.682A>G | NP_001387588.1:p.Asn228Asp | |
| NM_001400660.1:c.682A>G | NP_001387589.1:p.Asn228Asp | |
| NM_001400661.1:c.682A>G | NP_001387590.1:p.Asn228Asp | |
| NM_001400662.1:c.682A>G | NP_001387591.1:p.Asn228Asp | |
| NM_001400663.1:c.682A>G | NP_001387592.1:p.Asn228Asp | |
| NM_001400664.1:c.658A>G | NP_001387593.1:p.Asn220Asp | |
| NM_001400665.1:c.727+4117A>G | NP_001387594.1:n.727+4117A>G | |
| NM_001400666.1:c.595+3951A>G | NP_001387595.1:n.595+3951A>G | |
| NM_001400667.1:c.550+4117A>G | NP_001387596.1:n.550+4117A>G | |
| NM_001400668.1:c.550+4117A>G | NP_001387597.1:n.550+4117A>G | |
| NM_001400669.1:c.418A>G | NP_001387598.1:p.Asn140Asp | |
| NM_001400670.1:c.727A>G | NP_001387599.1:p.Asn243Asp | |
| NM_001400671.1:c.130A>G | NP_001387600.1:p.Asn44Asp | |
| NM_001400672.1:c.130A>G | NP_001387601.1:p.Asn44Asp | |
| NM_001400673.1:c.130A>G | NP_001387602.1:p.Asn44Asp | |
| NM_001400674.1:c.112A>G | NP_001387603.1:p.Asn38Asp | |
| NM_001400675.1:c.85A>G | NP_001387604.1:p.Asn29Asp | |
| NM_001400676.1:c.85A>G | NP_001387605.1:p.Asn29Asp | |
| NM_001400677.1:c.85A>G | NP_001387606.1:p.Asn29Asp | |
| NM_001400678.1:c.85A>G | NP_001387607.1:p.Asn29Asp | |
| NM_001400679.1:c.662A>G | NP_001387608.1:p.Gln221Arg | |
| NM_001400680.1:c.112A>G | NP_001387609.1:p.Asn38Asp | |
| NM_001400750.1:c.130A>G | NP_001387679.1:p.Asn44Asp | |
| NM_001400751.1:c.85A>G | NP_001387680.1:p.Asn29Asp | |
| NR_174564.1:n.680A>G | ||
| NR_174565.1:n.810A>G | ||
| NR_174581.1:n.836A>G | ||
| NR_174583.1:n.942A>G | ||
| NR_174584.1:n.991A>G | ||
| NR_174585.1:n.873A>G | ||
| NR_174586.1:n.847A>G | ||
| NR_174588.1:n.1010A>G | ||
| NR_174589.1:n.805A>G | ||
| NR_174590.1:n.897A>G | ||
| NR_174591.1:n.828A>G | ||
| NR_174592.1:n.1173A>G | ||
| NR_174593.1:n.971A>G | ||
| NR_174594.1:n.1014A>G | ||
| NR_174595.1:n.929A>G | ||
| NR_174596.1:n.766A>G | ||
| NR_174598.1:n.1124A>G | ||
| NR_174599.1:n.719+1940A>G | ||
| NR_174600.1:n.1036A>G | ||
| NR_174601.1:n.961A>G | ||
| NR_174602.1:n.831A>G |