Linked Data
ClinVar Variation Id:
1125473
ClinVar RCV Id:
RCV001457173
dbSNP Id:
rs780071959
ExAC:
16:2135305 G / T
gnomAD v2:
16-2135305-G-T
gnomAD v4:
16-2085304-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2085304G>T , CM000678.2:g.2085304G>T | GRCh38 |
| NC_000016.9:g.2135305G>T , CM000678.1:g.2135305G>T | GRCh37 |
| NC_000016.8:g.2075306G>T | NCBI36 |
| NG_005895.1:g.40999G>T , LRG_487:g.40999G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2993G>T | ENSP00000455997.2:n.*2993G>T | |
| ENST00000642206.2:c.4491G>T | ENSP00000495146.2:p.Leu1497= | |
| ENST00000642365.2:c.4641G>T | ENSP00000495459.2:p.Leu1547= | |
| ENST00000644417.2:c.*5024G>T | ENSP00000493912.2:n.*5024G>T | |
| ENST00000646464.2:c.*7393G>T | ENSP00000496610.2:n.*7393G>T | |
| ENST00000219476.9:c.4644G>T MANE Select | ENSP00000219476.3:p.Leu1548= | |
| ENST00000350773.9:c.4575G>T | ENSP00000344383.4:p.Leu1525= | |
| ENST00000401874.7:c.4443G>T | ENSP00000384468.2:p.Leu1481= | |
| ENST00000568454.6:c.4476G>T | ENSP00000454487.1:p.Leu1492= | |
| ENST00000569110.2:c.867G>T | ||
| ENST00000569930.2:n.2526G>T | ||
| ENST00000642365.1:c.3298G>T | ||
| ENST00000642561.1:c.4515G>T | ENSP00000495099.1:p.Leu1505= | |
| ENST00000642728.1:n.826G>T | ||
| ENST00000642791.1:n.241G>T | ||
| ENST00000642797.1:c.4446G>T | ENSP00000493846.1:p.Leu1482= | |
| ENST00000642936.1:c.4512G>T | ENSP00000494514.1:p.Leu1504= | |
| ENST00000643088.1:c.4437G>T | ENSP00000494747.1:p.Leu1479= | |
| ENST00000643177.1:n.658G>T | ||
| ENST00000643426.1:n.2292G>T | ||
| ENST00000643946.1:c.4569G>T | ENSP00000495927.1:p.Leu1523= | |
| ENST00000644043.1:c.4515G>T | ENSP00000496262.1:p.Leu1505= | |
| ENST00000644278.1:n.126G>T | ||
| ENST00000644329.1:c.4443G>T | ENSP00000496611.1:p.Leu1481= | |
| ENST00000644335.1:c.4440G>T | ENSP00000496317.1:p.Leu1480= | |
| ENST00000644399.1:c.4565G>T | ||
| ENST00000645024.1:n.2728G>T | ||
| ENST00000646388.1:c.4638G>T | ENSP00000495921.1:p.Leu1546= | |
| ENST00000646634.1:n.3459G>T | ||
| ENST00000646674.1:n.1896G>T | ||
| ENST00000647042.1:n.1867G>T | ||
| ENST00000647180.1:n.1757G>T | ||
| ENST00000219476.7:c.4644G>T | ENSP00000219476.3:p.Leu1548= | |
| ENST00000350773.8:c.4575G>T | ENSP00000344383.4:p.Leu1525= | |
| ENST00000382538.10:c.4299G>T | ENSP00000371978.6:p.Leu1433= | |
| ENST00000401874.6:c.4443G>T | ENSP00000384468.2:p.Leu1481= | |
| ENST00000439117.6:c.*3811G>T | ENSP00000406980.2:n.*3811G>T | |
| ENST00000439673.6:c.4335G>T | ENSP00000399232.2:p.Leu1445= | |
| ENST00000497886.5:n.2402G>T | ||
| ENST00000568454.5:c.4476G>T | ENSP00000454487.1:p.Leu1492= | |
| ENST00000569110.1:c.826G>T | ||
| ENST00000569930.1:n.1759G>T | ||
| NM_000548.3:c.4644G>T , LRG_487t1:c.4644G>T | NP_000539.2:p.Leu1548= | |
| NM_001077183.1:c.4443G>T | NP_001070651.1:p.Leu1481= | |
| NM_001114382.1:c.4575G>T | NP_001107854.1:p.Leu1525= | |
| XM_005255529.3:c.4515G>T | XP_005255586.2:p.Leu1505= | |
| XM_005255531.3:c.4446G>T | XP_005255588.2:p.Leu1482= | |
| XM_011522636.1:c.4698G>T | XP_011520938.1:p.Leu1566= | |
| XM_011522637.1:c.4695G>T | XP_011520939.1:p.Leu1565= | |
| XM_011522638.1:c.4587G>T | XP_011520940.1:p.Leu1529= | |
| XM_011522639.1:c.4569G>T | XP_011520941.1:p.Leu1523= | |
| XM_011522640.1:c.4566G>T | XP_011520942.1:p.Leu1522= | |
| XM_011522641.1:c.4335G>T | XP_011520943.1:p.Leu1445= | |
| NM_000548.4:c.4644G>T | NP_000539.2:p.Leu1548= | |
| NM_001077183.2:c.4443G>T | NP_001070651.1:p.Leu1481= | |
| NM_001114382.2:c.4575G>T | NP_001107854.1:p.Leu1525= | |
| NM_001318827.1:c.4335G>T | NP_001305756.1:p.Leu1445= | |
| NM_001318829.1:c.4299G>T | NP_001305758.1:p.Leu1433= | |
| NM_001318831.1:c.3912G>T | NP_001305760.1:p.Leu1304= | |
| NM_001318832.1:c.4476G>T | NP_001305761.1:p.Leu1492= | |
| NM_001363528.1:c.4446G>T | NP_001350457.1:p.Leu1482= | |
| NM_021055.2:c.4515G>T | NP_066399.2:p.Leu1505= | |
| XM_005255531.4:c.4446G>T | XP_005255588.2:p.Leu1482= | |
| XM_011522636.2:c.4698G>T | XP_011520938.1:p.Leu1566= | |
| XM_011522637.2:c.4695G>T | XP_011520939.1:p.Leu1565= | |
| XM_011522638.2:c.4860G>T | XP_011520940.2:p.Leu1620= | |
| XM_011522639.2:c.4569G>T | XP_011520941.1:p.Leu1523= | |
| XM_011522640.2:c.4566G>T | XP_011520942.1:p.Leu1522= | |
| XM_017023615.1:c.4641G>T | XP_016879104.1:p.Leu1547= | |
| XM_017023616.1:c.4512G>T | XP_016879105.1:p.Leu1504= | |
| XM_017023617.1:c.4608G>T | XP_016879106.1:p.Leu1536= | |
| XM_017023618.1:c.3354G>T | XP_016879107.1:p.Leu1118= | |
| XM_024450413.1:c.4443G>T | XP_024306181.1:p.Leu1481= | |
| NM_000548.5:c.4644G>T MANE Select | NP_000539.2:p.Leu1548= | |
| NM_001370404.1:c.4512G>T | NP_001357333.1:p.Leu1504= | |
| NM_001370405.1:c.4515G>T | NP_001357334.1:p.Leu1505= | |
| NM_001077183.3:c.4443G>T | NP_001070651.1:p.Leu1481= | |
| NM_001114382.3:c.4575G>T | NP_001107854.1:p.Leu1525= | |
| NM_001318827.2:c.4335G>T | NP_001305756.1:p.Leu1445= | |
| NM_001318829.2:c.4299G>T | NP_001305758.1:p.Leu1433= | |
| NM_001318831.2:c.3912G>T | NP_001305760.1:p.Leu1304= | |
| NM_001318832.2:c.4476G>T | NP_001305761.1:p.Leu1492= | |
| NM_001363528.2:c.4446G>T | NP_001350457.1:p.Leu1482= | |
| NM_021055.3:c.4515G>T | NP_066399.2:p.Leu1505= |