Linked Data
ClinVar Variation Id:
207785
dbSNP Id:
rs778925833
ExAC:
16:2134535 C / T
gnomAD v2:
16-2134535-C-T
gnomAD v3:
16-2084534-C-T
gnomAD v4:
16-2084534-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2084534C>T , CM000678.2:g.2084534C>T | GRCh38 |
| NC_000016.9:g.2134535C>T , CM000678.1:g.2134535C>T | GRCh37 |
| NC_000016.8:g.2074536C>T | NCBI36 |
| NG_005895.1:g.40229C>T , LRG_487:g.40229C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2661C>T | ENSP00000455997.2:n.*2661C>T | |
| ENST00000642206.2:c.4159C>T | ENSP00000495146.2:p.Arg1387Trp | |
| ENST00000642365.2:c.4309C>T | ENSP00000495459.2:p.Arg1437Trp | |
| ENST00000644417.2:c.*4692C>T | ENSP00000493912.2:n.*4692C>T | |
| ENST00000646464.2:c.*7061C>T | ENSP00000496610.2:n.*7061C>T | |
| ENST00000219476.9:c.4312C>T MANE Select | ENSP00000219476.3:p.Arg1438Trp | |
| ENST00000350773.9:c.4243C>T | ENSP00000344383.4:p.Arg1415Trp | |
| ENST00000401874.7:c.4111C>T | ENSP00000384468.2:p.Arg1371Trp | |
| ENST00000568454.6:c.4144C>T | ENSP00000454487.1:p.Arg1382Trp | |
| ENST00000569110.2:c.548C>T | ||
| ENST00000569930.2:n.2194C>T | ||
| ENST00000642365.1:c.2966C>T | ||
| ENST00000642561.1:c.4183C>T | ENSP00000495099.1:p.Arg1395Trp | |
| ENST00000642728.1:n.494C>T | ||
| ENST00000642797.1:c.4114C>T | ENSP00000493846.1:p.Arg1372Trp | |
| ENST00000642936.1:c.4180C>T | ENSP00000494514.1:p.Arg1394Trp | |
| ENST00000643088.1:c.4111C>T | ENSP00000494747.1:p.Arg1371Trp | |
| ENST00000643177.1:n.326C>T | ||
| ENST00000643426.1:n.1960C>T | ||
| ENST00000643946.1:c.4243C>T | ENSP00000495927.1:p.Arg1415Trp | |
| ENST00000644043.1:c.4183C>T | ENSP00000496262.1:p.Arg1395Trp | |
| ENST00000644329.1:c.4111C>T | ENSP00000496611.1:p.Arg1371Trp | |
| ENST00000644335.1:c.4114C>T | ENSP00000496317.1:p.Arg1372Trp | |
| ENST00000644399.1:c.4233C>T | ||
| ENST00000645024.1:n.2396C>T | ||
| ENST00000646388.1:c.4312C>T | ENSP00000495921.1:p.Arg1438Trp | |
| ENST00000646634.1:n.3127C>T | ||
| ENST00000646674.1:n.1564C>T | ||
| ENST00000647042.1:n.1535C>T | ||
| ENST00000647180.1:n.1425C>T | ||
| ENST00000219476.7:c.4312C>T | ENSP00000219476.3:p.Arg1438Trp | |
| ENST00000350773.8:c.4243C>T | ENSP00000344383.4:p.Arg1415Trp | |
| ENST00000382538.10:c.3967C>T | ENSP00000371978.6:p.Arg1323Trp | |
| ENST00000401874.6:c.4111C>T | ENSP00000384468.2:p.Arg1371Trp | |
| ENST00000439117.6:c.*3479C>T | ENSP00000406980.2:n.*3479C>T | |
| ENST00000439673.6:c.4003C>T | ENSP00000399232.2:p.Arg1335Trp | |
| ENST00000497886.5:n.2070C>T | ||
| ENST00000568454.5:c.4144C>T | ENSP00000454487.1:p.Arg1382Trp | |
| ENST00000569110.1:c.494C>T | ||
| ENST00000569930.1:n.1427C>T | ||
| NM_000548.3:c.4312C>T , LRG_487t1:c.4312C>T | NP_000539.2:p.Arg1438Trp | |
| NM_001077183.1:c.4111C>T | NP_001070651.1:p.Arg1371Trp | |
| NM_001114382.1:c.4243C>T | NP_001107854.1:p.Arg1415Trp | |
| XM_005255529.3:c.4183C>T | XP_005255586.2:p.Arg1395Trp | |
| XM_005255531.3:c.4114C>T | XP_005255588.2:p.Arg1372Trp | |
| XM_011522636.1:c.4366C>T | XP_011520938.1:p.Arg1456Trp | |
| XM_011522637.1:c.4363C>T | XP_011520939.1:p.Arg1455Trp | |
| XM_011522638.1:c.4255C>T | XP_011520940.1:p.Arg1419Trp | |
| XM_011522639.1:c.4237C>T | XP_011520941.1:p.Arg1413Trp | |
| XM_011522640.1:c.4234C>T | XP_011520942.1:p.Arg1412Trp | |
| XM_011522641.1:c.4003C>T | XP_011520943.1:p.Arg1335Trp | |
| NM_000548.4:c.4312C>T | NP_000539.2:p.Arg1438Trp | |
| NM_001077183.2:c.4111C>T | NP_001070651.1:p.Arg1371Trp | |
| NM_001114382.2:c.4243C>T | NP_001107854.1:p.Arg1415Trp | |
| NM_001318827.1:c.4003C>T | NP_001305756.1:p.Arg1335Trp | |
| NM_001318829.1:c.3967C>T | NP_001305758.1:p.Arg1323Trp | |
| NM_001318831.1:c.3580C>T | NP_001305760.1:p.Arg1194Trp | |
| NM_001318832.1:c.4144C>T | NP_001305761.1:p.Arg1382Trp | |
| NM_001363528.1:c.4114C>T | NP_001350457.1:p.Arg1372Trp | |
| NM_021055.2:c.4183C>T | NP_066399.2:p.Arg1395Trp | |
| XM_005255531.4:c.4114C>T | XP_005255588.2:p.Arg1372Trp | |
| XM_011522636.2:c.4366C>T | XP_011520938.1:p.Arg1456Trp | |
| XM_011522637.2:c.4363C>T | XP_011520939.1:p.Arg1455Trp | |
| XM_011522638.2:c.4528C>T | XP_011520940.2:p.Arg1510Trp | |
| XM_011522639.2:c.4237C>T | XP_011520941.1:p.Arg1413Trp | |
| XM_011522640.2:c.4234C>T | XP_011520942.1:p.Arg1412Trp | |
| XM_017023615.1:c.4309C>T | XP_016879104.1:p.Arg1437Trp | |
| XM_017023616.1:c.4180C>T | XP_016879105.1:p.Arg1394Trp | |
| XM_017023617.1:c.4276C>T | XP_016879106.1:p.Arg1426Trp | |
| XM_017023618.1:c.3022C>T | XP_016879107.1:p.Arg1008Trp | |
| XM_024450413.1:c.4111C>T | XP_024306181.1:p.Arg1371Trp | |
| NM_000548.5:c.4312C>T MANE Select | NP_000539.2:p.Arg1438Trp | |
| NM_001370404.1:c.4180C>T | NP_001357333.1:p.Arg1394Trp | |
| NM_001370405.1:c.4183C>T | NP_001357334.1:p.Arg1395Trp | |
| NM_001077183.3:c.4111C>T | NP_001070651.1:p.Arg1371Trp | |
| NM_001114382.3:c.4243C>T | NP_001107854.1:p.Arg1415Trp | |
| NM_001318827.2:c.4003C>T | NP_001305756.1:p.Arg1335Trp | |
| NM_001318829.2:c.3967C>T | NP_001305758.1:p.Arg1323Trp | |
| NM_001318831.2:c.3580C>T | NP_001305760.1:p.Arg1194Trp | |
| NM_001318832.2:c.4144C>T | NP_001305761.1:p.Arg1382Trp | |
| NM_001363528.2:c.4114C>T | NP_001350457.1:p.Arg1372Trp | |
| NM_021055.3:c.4183C>T | NP_066399.2:p.Arg1395Trp |