Linked Data
ClinVar Variation Id:
468098
dbSNP Id:
rs764903148
ExAC:
16:2135010 A / G
gnomAD v2:
16-2135010-A-G
gnomAD v3:
16-2085009-A-G
gnomAD v4:
16-2085009-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2085009A>G , CM000678.2:g.2085009A>G | GRCh38 |
| NC_000016.9:g.2135010A>G , CM000678.1:g.2135010A>G | GRCh37 |
| NC_000016.8:g.2075011A>G | NCBI36 |
| NG_005895.1:g.40704A>G , LRG_487:g.40704A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2901A>G | ENSP00000455997.2:n.*2901A>G | |
| ENST00000642206.2:c.4399A>G | ENSP00000495146.2:p.Ile1467Val | |
| ENST00000642365.2:c.4549A>G | ENSP00000495459.2:p.Ile1517Val | |
| ENST00000644417.2:c.*4932A>G | ENSP00000493912.2:n.*4932A>G | |
| ENST00000646464.2:c.*7301A>G | ENSP00000496610.2:n.*7301A>G | |
| ENST00000219476.9:c.4552A>G MANE Select | ENSP00000219476.3:p.Ile1518Val | |
| ENST00000350773.9:c.4483A>G | ENSP00000344383.4:p.Ile1495Val | |
| ENST00000401874.7:c.4351A>G | ENSP00000384468.2:p.Ile1451Val | |
| ENST00000568454.6:c.4384A>G | ENSP00000454487.1:p.Ile1462Val | |
| ENST00000569110.2:c.775A>G | ||
| ENST00000569930.2:n.2434A>G | ||
| ENST00000642365.1:c.3206A>G | ||
| ENST00000642561.1:c.4423A>G | ENSP00000495099.1:p.Ile1475Val | |
| ENST00000642728.1:n.734A>G | ||
| ENST00000642797.1:c.4354A>G | ENSP00000493846.1:p.Ile1452Val | |
| ENST00000642936.1:c.4420A>G | ENSP00000494514.1:p.Ile1474Val | |
| ENST00000643088.1:c.4351A>G | ENSP00000494747.1:p.Ile1451Val | |
| ENST00000643177.1:n.566A>G | ||
| ENST00000643426.1:n.2200A>G | ||
| ENST00000643946.1:c.4483A>G | ENSP00000495927.1:p.Ile1495Val | |
| ENST00000644043.1:c.4423A>G | ENSP00000496262.1:p.Ile1475Val | |
| ENST00000644329.1:c.4351A>G | ENSP00000496611.1:p.Ile1451Val | |
| ENST00000644335.1:c.4354A>G | ENSP00000496317.1:p.Ile1452Val | |
| ENST00000644399.1:c.4473A>G | ||
| ENST00000645024.1:n.2636A>G | ||
| ENST00000646388.1:c.4552A>G | ENSP00000495921.1:p.Ile1518Val | |
| ENST00000646634.1:n.3367A>G | ||
| ENST00000646674.1:n.1804A>G | ||
| ENST00000647042.1:n.1775A>G | ||
| ENST00000647180.1:n.1665A>G | ||
| ENST00000219476.7:c.4552A>G | ENSP00000219476.3:p.Ile1518Val | |
| ENST00000350773.8:c.4483A>G | ENSP00000344383.4:p.Ile1495Val | |
| ENST00000382538.10:c.4207A>G | ENSP00000371978.6:p.Ile1403Val | |
| ENST00000401874.6:c.4351A>G | ENSP00000384468.2:p.Ile1451Val | |
| ENST00000439117.6:c.*3719A>G | ENSP00000406980.2:n.*3719A>G | |
| ENST00000439673.6:c.4243A>G | ENSP00000399232.2:p.Ile1415Val | |
| ENST00000497886.5:n.2310A>G | ||
| ENST00000568454.5:c.4384A>G | ENSP00000454487.1:p.Ile1462Val | |
| ENST00000569110.1:c.734A>G | ||
| ENST00000569930.1:n.1667A>G | ||
| NM_000548.3:c.4552A>G , LRG_487t1:c.4552A>G | NP_000539.2:p.Ile1518Val | |
| NM_001077183.1:c.4351A>G | NP_001070651.1:p.Ile1451Val | |
| NM_001114382.1:c.4483A>G | NP_001107854.1:p.Ile1495Val | |
| XM_005255529.3:c.4423A>G | XP_005255586.2:p.Ile1475Val | |
| XM_005255531.3:c.4354A>G | XP_005255588.2:p.Ile1452Val | |
| XM_011522636.1:c.4606A>G | XP_011520938.1:p.Ile1536Val | |
| XM_011522637.1:c.4603A>G | XP_011520939.1:p.Ile1535Val | |
| XM_011522638.1:c.4495A>G | XP_011520940.1:p.Ile1499Val | |
| XM_011522639.1:c.4477A>G | XP_011520941.1:p.Ile1493Val | |
| XM_011522640.1:c.4474A>G | XP_011520942.1:p.Ile1492Val | |
| XM_011522641.1:c.4243A>G | XP_011520943.1:p.Ile1415Val | |
| NM_000548.4:c.4552A>G | NP_000539.2:p.Ile1518Val | |
| NM_001077183.2:c.4351A>G | NP_001070651.1:p.Ile1451Val | |
| NM_001114382.2:c.4483A>G | NP_001107854.1:p.Ile1495Val | |
| NM_001318827.1:c.4243A>G | NP_001305756.1:p.Ile1415Val | |
| NM_001318829.1:c.4207A>G | NP_001305758.1:p.Ile1403Val | |
| NM_001318831.1:c.3820A>G | NP_001305760.1:p.Ile1274Val | |
| NM_001318832.1:c.4384A>G | NP_001305761.1:p.Ile1462Val | |
| NM_001363528.1:c.4354A>G | NP_001350457.1:p.Ile1452Val | |
| NM_021055.2:c.4423A>G | NP_066399.2:p.Ile1475Val | |
| XM_005255531.4:c.4354A>G | XP_005255588.2:p.Ile1452Val | |
| XM_011522636.2:c.4606A>G | XP_011520938.1:p.Ile1536Val | |
| XM_011522637.2:c.4603A>G | XP_011520939.1:p.Ile1535Val | |
| XM_011522638.2:c.4768A>G | XP_011520940.2:p.Ile1590Val | |
| XM_011522639.2:c.4477A>G | XP_011520941.1:p.Ile1493Val | |
| XM_011522640.2:c.4474A>G | XP_011520942.1:p.Ile1492Val | |
| XM_017023615.1:c.4549A>G | XP_016879104.1:p.Ile1517Val | |
| XM_017023616.1:c.4420A>G | XP_016879105.1:p.Ile1474Val | |
| XM_017023617.1:c.4516A>G | XP_016879106.1:p.Ile1506Val | |
| XM_017023618.1:c.3262A>G | XP_016879107.1:p.Ile1088Val | |
| XM_024450413.1:c.4351A>G | XP_024306181.1:p.Ile1451Val | |
| NM_000548.5:c.4552A>G MANE Select | NP_000539.2:p.Ile1518Val | |
| NM_001370404.1:c.4420A>G | NP_001357333.1:p.Ile1474Val | |
| NM_001370405.1:c.4423A>G | NP_001357334.1:p.Ile1475Val | |
| NM_001077183.3:c.4351A>G | NP_001070651.1:p.Ile1451Val | |
| NM_001114382.3:c.4483A>G | NP_001107854.1:p.Ile1495Val | |
| NM_001318827.2:c.4243A>G | NP_001305756.1:p.Ile1415Val | |
| NM_001318829.2:c.4207A>G | NP_001305758.1:p.Ile1403Val | |
| NM_001318831.2:c.3820A>G | NP_001305760.1:p.Ile1274Val | |
| NM_001318832.2:c.4384A>G | NP_001305761.1:p.Ile1462Val | |
| NM_001363528.2:c.4354A>G | NP_001350457.1:p.Ile1452Val | |
| NM_021055.3:c.4423A>G | NP_066399.2:p.Ile1475Val |