Linked Data
ClinVar Variation Id:
220843
dbSNP Id:
rs201038907
ExAC:
16:2135278 A / G
gnomAD v2:
16-2135278-A-G
gnomAD v3:
16-2085277-A-G
gnomAD v4:
16-2085277-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2085277A>G , CM000678.2:g.2085277A>G | GRCh38 |
| NC_000016.9:g.2135278A>G , CM000678.1:g.2135278A>G | GRCh37 |
| NC_000016.8:g.2075279A>G | NCBI36 |
| NG_005895.1:g.40972A>G , LRG_487:g.40972A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2966A>G | ENSP00000455997.2:n.*2966A>G | |
| ENST00000642206.2:c.4464A>G | ENSP00000495146.2:p.Ser1488= | |
| ENST00000642365.2:c.4614A>G | ENSP00000495459.2:p.Ser1538= | |
| ENST00000644417.2:c.*4997A>G | ENSP00000493912.2:n.*4997A>G | |
| ENST00000646464.2:c.*7366A>G | ENSP00000496610.2:n.*7366A>G | |
| ENST00000219476.9:c.4617A>G MANE Select | ENSP00000219476.3:p.Ser1539= | |
| ENST00000350773.9:c.4548A>G | ENSP00000344383.4:p.Ser1516= | |
| ENST00000401874.7:c.4416A>G | ENSP00000384468.2:p.Ser1472= | |
| ENST00000568454.6:c.4449A>G | ENSP00000454487.1:p.Ser1483= | |
| ENST00000569110.2:c.840A>G | ||
| ENST00000569930.2:n.2499A>G | ||
| ENST00000642365.1:c.3271A>G | ||
| ENST00000642561.1:c.4488A>G | ENSP00000495099.1:p.Ser1496= | |
| ENST00000642728.1:n.799A>G | ||
| ENST00000642791.1:n.214A>G | ||
| ENST00000642797.1:c.4419A>G | ENSP00000493846.1:p.Ser1473= | |
| ENST00000642936.1:c.4485A>G | ENSP00000494514.1:p.Ser1495= | |
| ENST00000643088.1:c.4410A>G | ENSP00000494747.1:p.Ser1470= | |
| ENST00000643177.1:n.631A>G | ||
| ENST00000643426.1:n.2265A>G | ||
| ENST00000643946.1:c.4542A>G | ENSP00000495927.1:p.Ser1514= | |
| ENST00000644043.1:c.4488A>G | ENSP00000496262.1:p.Ser1496= | |
| ENST00000644278.1:n.99A>G | ||
| ENST00000644329.1:c.4416A>G | ENSP00000496611.1:p.Ser1472= | |
| ENST00000644335.1:c.4413A>G | ENSP00000496317.1:p.Ser1471= | |
| ENST00000644399.1:c.4538A>G | ||
| ENST00000645024.1:n.2701A>G | ||
| ENST00000646388.1:c.4611A>G | ENSP00000495921.1:p.Ser1537= | |
| ENST00000646634.1:n.3432A>G | ||
| ENST00000646674.1:n.1869A>G | ||
| ENST00000647042.1:n.1840A>G | ||
| ENST00000647180.1:n.1730A>G | ||
| ENST00000219476.7:c.4617A>G | ENSP00000219476.3:p.Ser1539= | |
| ENST00000350773.8:c.4548A>G | ENSP00000344383.4:p.Ser1516= | |
| ENST00000382538.10:c.4272A>G | ENSP00000371978.6:p.Ser1424= | |
| ENST00000401874.6:c.4416A>G | ENSP00000384468.2:p.Ser1472= | |
| ENST00000439117.6:c.*3784A>G | ENSP00000406980.2:n.*3784A>G | |
| ENST00000439673.6:c.4308A>G | ENSP00000399232.2:p.Ser1436= | |
| ENST00000497886.5:n.2375A>G | ||
| ENST00000568454.5:c.4449A>G | ENSP00000454487.1:p.Ser1483= | |
| ENST00000569110.1:c.799A>G | ||
| ENST00000569930.1:n.1732A>G | ||
| NM_000548.3:c.4617A>G , LRG_487t1:c.4617A>G | NP_000539.2:p.Ser1539= | |
| NM_001077183.1:c.4416A>G | NP_001070651.1:p.Ser1472= | |
| NM_001114382.1:c.4548A>G | NP_001107854.1:p.Ser1516= | |
| XM_005255529.3:c.4488A>G | XP_005255586.2:p.Ser1496= | |
| XM_005255531.3:c.4419A>G | XP_005255588.2:p.Ser1473= | |
| XM_011522636.1:c.4671A>G | XP_011520938.1:p.Ser1557= | |
| XM_011522637.1:c.4668A>G | XP_011520939.1:p.Ser1556= | |
| XM_011522638.1:c.4560A>G | XP_011520940.1:p.Ser1520= | |
| XM_011522639.1:c.4542A>G | XP_011520941.1:p.Ser1514= | |
| XM_011522640.1:c.4539A>G | XP_011520942.1:p.Ser1513= | |
| XM_011522641.1:c.4308A>G | XP_011520943.1:p.Ser1436= | |
| NM_000548.4:c.4617A>G | NP_000539.2:p.Ser1539= | |
| NM_001077183.2:c.4416A>G | NP_001070651.1:p.Ser1472= | |
| NM_001114382.2:c.4548A>G | NP_001107854.1:p.Ser1516= | |
| NM_001318827.1:c.4308A>G | NP_001305756.1:p.Ser1436= | |
| NM_001318829.1:c.4272A>G | NP_001305758.1:p.Ser1424= | |
| NM_001318831.1:c.3885A>G | NP_001305760.1:p.Ser1295= | |
| NM_001318832.1:c.4449A>G | NP_001305761.1:p.Ser1483= | |
| NM_001363528.1:c.4419A>G | NP_001350457.1:p.Ser1473= | |
| NM_021055.2:c.4488A>G | NP_066399.2:p.Ser1496= | |
| XM_005255531.4:c.4419A>G | XP_005255588.2:p.Ser1473= | |
| XM_011522636.2:c.4671A>G | XP_011520938.1:p.Ser1557= | |
| XM_011522637.2:c.4668A>G | XP_011520939.1:p.Ser1556= | |
| XM_011522638.2:c.4833A>G | XP_011520940.2:p.Ser1611= | |
| XM_011522639.2:c.4542A>G | XP_011520941.1:p.Ser1514= | |
| XM_011522640.2:c.4539A>G | XP_011520942.1:p.Ser1513= | |
| XM_017023615.1:c.4614A>G | XP_016879104.1:p.Ser1538= | |
| XM_017023616.1:c.4485A>G | XP_016879105.1:p.Ser1495= | |
| XM_017023617.1:c.4581A>G | XP_016879106.1:p.Ser1527= | |
| XM_017023618.1:c.3327A>G | XP_016879107.1:p.Ser1109= | |
| XM_024450413.1:c.4416A>G | XP_024306181.1:p.Ser1472= | |
| NM_000548.5:c.4617A>G MANE Select | NP_000539.2:p.Ser1539= | |
| NM_001370404.1:c.4485A>G | NP_001357333.1:p.Ser1495= | |
| NM_001370405.1:c.4488A>G | NP_001357334.1:p.Ser1496= | |
| NM_001077183.3:c.4416A>G | NP_001070651.1:p.Ser1472= | |
| NM_001114382.3:c.4548A>G | NP_001107854.1:p.Ser1516= | |
| NM_001318827.2:c.4308A>G | NP_001305756.1:p.Ser1436= | |
| NM_001318829.2:c.4272A>G | NP_001305758.1:p.Ser1424= | |
| NM_001318831.2:c.3885A>G | NP_001305760.1:p.Ser1295= | |
| NM_001318832.2:c.4449A>G | NP_001305761.1:p.Ser1483= | |
| NM_001363528.2:c.4419A>G | NP_001350457.1:p.Ser1473= | |
| NM_021055.3:c.4488A>G | NP_066399.2:p.Ser1496= |