Linked Data
ClinVar Variation Id:
468039
dbSNP Id:
rs765255206
ExAC:
16:2131770 A / G
gnomAD v2:
16-2131770-A-G
gnomAD v4:
16-2081769-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2081769A>G , CM000678.2:g.2081769A>G | GRCh38 |
| NC_000016.9:g.2131770A>G , CM000678.1:g.2131770A>G | GRCh37 |
| NC_000016.8:g.2071771A>G | NCBI36 |
| NG_005895.1:g.37464A>G , LRG_487:g.37464A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2203A>G | ENSP00000455997.2:n.*2203A>G | |
| ENST00000642206.2:c.3701A>G | ENSP00000495146.2:p.Lys1234Arg | |
| ENST00000642365.2:c.3782A>G | ENSP00000495459.2:p.Lys1261Arg | |
| ENST00000644417.2:c.*4234A>G | ENSP00000493912.2:n.*4234A>G | |
| ENST00000646464.2:c.*4707A>G | ENSP00000496610.2:n.*4707A>G | |
| ENST00000219476.9:c.3785A>G MANE Select | ENSP00000219476.3:p.Lys1262Arg | |
| ENST00000350773.9:c.3785A>G | ENSP00000344383.4:p.Lys1262Arg | |
| ENST00000401874.7:c.3653A>G | ENSP00000384468.2:p.Lys1218Arg | |
| ENST00000568454.6:c.3686A>G | ENSP00000454487.1:p.Lys1229Arg | |
| ENST00000642365.1:c.2439A>G | ||
| ENST00000642561.1:c.3656A>G | ENSP00000495099.1:p.Lys1219Arg | |
| ENST00000642797.1:c.3656A>G | ENSP00000493846.1:p.Lys1219Arg | |
| ENST00000642936.1:c.3653A>G | ENSP00000494514.1:p.Lys1218Arg | |
| ENST00000643088.1:c.3653A>G | ENSP00000494747.1:p.Lys1218Arg | |
| ENST00000643426.1:n.1433A>G | ||
| ENST00000643533.1:n.295A>G | ||
| ENST00000643946.1:c.3785A>G | ENSP00000495927.1:p.Lys1262Arg | |
| ENST00000644043.1:c.3656A>G | ENSP00000496262.1:p.Lys1219Arg | |
| ENST00000644329.1:c.3653A>G | ENSP00000496611.1:p.Lys1218Arg | |
| ENST00000644335.1:c.3656A>G | ENSP00000496317.1:p.Lys1219Arg | |
| ENST00000644399.1:c.3775A>G | ||
| ENST00000644722.1:n.931A>G | ||
| ENST00000645024.1:n.1938A>G | ||
| ENST00000646388.1:c.3785A>G | ENSP00000495921.1:p.Lys1262Arg | |
| ENST00000646634.1:n.2669A>G | ||
| ENST00000646674.1:n.400A>G | ||
| ENST00000647042.1:n.1077A>G | ||
| ENST00000647180.1:n.265A>G | ||
| ENST00000219476.7:c.3785A>G | ENSP00000219476.3:p.Lys1262Arg | |
| ENST00000350773.8:c.3785A>G | ENSP00000344383.4:p.Lys1262Arg | |
| ENST00000382538.10:c.3509A>G | ENSP00000371978.6:p.Lys1170Arg | |
| ENST00000401874.6:c.3653A>G | ENSP00000384468.2:p.Lys1218Arg | |
| ENST00000439117.6:c.*2952A>G | ENSP00000406980.2:n.*2952A>G | |
| ENST00000439673.6:c.3545A>G | ENSP00000399232.2:p.Lys1182Arg | |
| ENST00000497886.5:n.1612A>G | ||
| ENST00000568454.5:c.3686A>G | ENSP00000454487.1:p.Lys1229Arg | |
| NM_000548.3:c.3785A>G , LRG_487t1:c.3785A>G | NP_000539.2:p.Lys1262Arg | |
| NM_001077183.1:c.3653A>G | NP_001070651.1:p.Lys1218Arg | |
| NM_001114382.1:c.3785A>G | NP_001107854.1:p.Lys1262Arg | |
| XM_005255529.3:c.3656A>G | XP_005255586.2:p.Lys1219Arg | |
| XM_005255531.3:c.3656A>G | XP_005255588.2:p.Lys1219Arg | |
| XM_011522636.1:c.3785A>G | XP_011520938.1:p.Lys1262Arg | |
| XM_011522637.1:c.3782A>G | XP_011520939.1:p.Lys1261Arg | |
| XM_011522638.1:c.3674A>G | XP_011520940.1:p.Lys1225Arg | |
| XM_011522639.1:c.3656A>G | XP_011520941.1:p.Lys1219Arg | |
| XM_011522640.1:c.3653A>G | XP_011520942.1:p.Lys1218Arg | |
| XM_011522641.1:c.3545A>G | XP_011520943.1:p.Lys1182Arg | |
| NM_000548.4:c.3785A>G | NP_000539.2:p.Lys1262Arg | |
| NM_001077183.2:c.3653A>G | NP_001070651.1:p.Lys1218Arg | |
| NM_001114382.2:c.3785A>G | NP_001107854.1:p.Lys1262Arg | |
| NM_001318827.1:c.3545A>G | NP_001305756.1:p.Lys1182Arg | |
| NM_001318829.1:c.3509A>G | NP_001305758.1:p.Lys1170Arg | |
| NM_001318831.1:c.3053A>G | NP_001305760.1:p.Lys1018Arg | |
| NM_001318832.1:c.3686A>G | NP_001305761.1:p.Lys1229Arg | |
| NM_001363528.1:c.3656A>G | NP_001350457.1:p.Lys1219Arg | |
| NM_021055.2:c.3656A>G | NP_066399.2:p.Lys1219Arg | |
| XM_005255531.4:c.3656A>G | XP_005255588.2:p.Lys1219Arg | |
| XM_011522636.2:c.3785A>G | XP_011520938.1:p.Lys1262Arg | |
| XM_011522637.2:c.3782A>G | XP_011520939.1:p.Lys1261Arg | |
| XM_011522638.2:c.3947A>G | XP_011520940.2:p.Lys1316Arg | |
| XM_011522639.2:c.3656A>G | XP_011520941.1:p.Lys1219Arg | |
| XM_011522640.2:c.3653A>G | XP_011520942.1:p.Lys1218Arg | |
| XM_017023615.1:c.3782A>G | XP_016879104.1:p.Lys1261Arg | |
| XM_017023616.1:c.3653A>G | XP_016879105.1:p.Lys1218Arg | |
| XM_017023617.1:c.3818A>G | XP_016879106.1:p.Lys1273Arg | |
| XM_017023618.1:c.2441A>G | XP_016879107.1:p.Lys814Arg | |
| XM_024450413.1:c.3653A>G | XP_024306181.1:p.Lys1218Arg | |
| NM_000548.5:c.3785A>G MANE Select | NP_000539.2:p.Lys1262Arg | |
| NM_001370404.1:c.3653A>G | NP_001357333.1:p.Lys1218Arg | |
| NM_001370405.1:c.3656A>G | NP_001357334.1:p.Lys1219Arg | |
| NM_001077183.3:c.3653A>G | NP_001070651.1:p.Lys1218Arg | |
| NM_001114382.3:c.3785A>G | NP_001107854.1:p.Lys1262Arg | |
| NM_001318827.2:c.3545A>G | NP_001305756.1:p.Lys1182Arg | |
| NM_001318829.2:c.3509A>G | NP_001305758.1:p.Lys1170Arg | |
| NM_001318831.2:c.3053A>G | NP_001305760.1:p.Lys1018Arg | |
| NM_001318832.2:c.3686A>G | NP_001305761.1:p.Lys1229Arg | |
| NM_001363528.2:c.3656A>G | NP_001350457.1:p.Lys1219Arg | |
| NM_021055.3:c.3656A>G | NP_066399.2:p.Lys1219Arg |