Linked Data
ClinVar Variation Id:
381254
dbSNP Id:
rs372463702
ExAC:
16:2108881 C / T
gnomAD v2:
16-2108881-C-T
gnomAD v3:
16-2058880-C-T
gnomAD v4:
16-2058880-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2058880C>T , CM000678.2:g.2058880C>T | GRCh38 |
| NC_000016.9:g.2108881C>T , CM000678.1:g.2108881C>T | GRCh37 |
| NC_000016.8:g.2048882C>T | NCBI36 |
| NG_005895.1:g.14575C>T , LRG_487:g.14575C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.975+7C>T | ENSP00000455997.2:n.975+7C>T | |
| ENST00000642206.2:c.1020+7C>T | ENSP00000495146.2:n.1020+7C>T | |
| ENST00000642365.2:c.975+7C>T | ENSP00000495459.2:n.975+7C>T | |
| ENST00000644417.2:c.*412+7C>T | ENSP00000493912.2:n.*412+7C>T | |
| ENST00000646464.2:c.*580+7C>T | ENSP00000496610.2:n.*580+7C>T | |
| ENST00000219476.9:c.975+7C>T MANE Select | ENSP00000219476.3:n.975+7C>T | |
| ENST00000350773.9:c.975+7C>T | ENSP00000344383.4:n.975+7C>T | |
| ENST00000401874.7:c.975+7C>T | ENSP00000384468.2:n.975+7C>T | |
| ENST00000467949.2:n.427+7C>T | ||
| ENST00000568454.6:c.1008+7C>T | ENSP00000454487.1:n.1008+7C>T | |
| ENST00000642561.1:c.975+7C>T | ENSP00000495099.1:n.975+7C>T | |
| ENST00000642797.1:c.975+7C>T | ENSP00000493846.1:n.975+7C>T | |
| ENST00000642812.1:n.1020+7C>T | ||
| ENST00000642936.1:c.975+7C>T | ENSP00000494514.1:n.975+7C>T | |
| ENST00000643088.1:c.975+7C>T | ENSP00000494747.1:n.975+7C>T | |
| ENST00000643149.1:n.1928+7C>T | ||
| ENST00000643298.1:c.*477+7C>T | ENSP00000494393.1:n.*477+7C>T | |
| ENST00000643745.1:c.975+7C>T | ENSP00000495948.1:n.975+7C>T | |
| ENST00000643946.1:c.975+7C>T | ENSP00000495927.1:n.975+7C>T | |
| ENST00000644043.1:c.975+7C>T | ENSP00000496262.1:n.975+7C>T | |
| ENST00000644135.1:c.975+7C>T | ENSP00000495644.1:n.975+7C>T | |
| ENST00000644222.1:n.1062+7C>T | ||
| ENST00000644329.1:c.975+7C>T | ENSP00000496611.1:n.975+7C>T | |
| ENST00000644335.1:c.975+7C>T | ENSP00000496317.1:n.975+7C>T | |
| ENST00000644399.1:c.968+7C>T | ||
| ENST00000644665.1:n.1092+7C>T | ||
| ENST00000645591.1:n.1946+7C>T | ||
| ENST00000646388.1:c.975+7C>T | ENSP00000495921.1:n.975+7C>T | |
| ENST00000646823.1:n.1389+7C>T | ||
| ENST00000647234.1:n.1676+7C>T | ||
| ENST00000647242.1:n.1643+7C>T | ||
| ENST00000219476.7:c.975+7C>T | ENSP00000219476.3:n.975+7C>T | |
| ENST00000350773.8:c.975+7C>T | ENSP00000344383.4:n.975+7C>T | |
| ENST00000382538.10:c.828+7C>T | ENSP00000371978.6:n.828+7C>T | |
| ENST00000401874.6:c.975+7C>T | ENSP00000384468.2:n.975+7C>T | |
| ENST00000439117.6:c.*274+7C>T | ENSP00000406980.2:n.*274+7C>T | |
| ENST00000439673.6:c.864+7C>T | ENSP00000399232.2:n.864+7C>T | |
| ENST00000467949.1:c.411+7C>T | ENSP00000454997.1:n.411+7C>T | |
| ENST00000568454.5:c.1008+7C>T | ENSP00000454487.1:n.1008+7C>T | |
| NM_000548.3:c.975+7C>T , LRG_487t1:c.975+7C>T | NP_000539.2:n.975+7C>T | |
| NM_001077183.1:c.975+7C>T | NP_001070651.1:n.975+7C>T | |
| NM_001114382.1:c.975+7C>T | NP_001107854.1:n.975+7C>T | |
| XM_005255529.3:c.975+7C>T | XP_005255586.2:n.975+7C>T | |
| XM_005255531.3:c.975+7C>T | XP_005255588.2:n.975+7C>T | |
| XM_011522636.1:c.975+7C>T | XP_011520938.1:n.975+7C>T | |
| XM_011522637.1:c.975+7C>T | XP_011520939.1:n.975+7C>T | |
| XM_011522638.1:c.864+7C>T | XP_011520940.1:n.864+7C>T | |
| XM_011522639.1:c.975+7C>T | XP_011520941.1:n.975+7C>T | |
| XM_011522640.1:c.975+7C>T | XP_011520942.1:n.975+7C>T | |
| XM_011522641.1:c.864+7C>T | XP_011520943.1:n.864+7C>T | |
| NM_000548.4:c.975+7C>T | NP_000539.2:n.975+7C>T | |
| NM_001077183.2:c.975+7C>T | NP_001070651.1:n.975+7C>T | |
| NM_001114382.2:c.975+7C>T | NP_001107854.1:n.975+7C>T | |
| NM_001318827.1:c.864+7C>T | NP_001305756.1:n.864+7C>T | |
| NM_001318829.1:c.828+7C>T | NP_001305758.1:n.828+7C>T | |
| NM_001318831.1:c.375+7C>T | NP_001305760.1:n.375+7C>T | |
| NM_001318832.1:c.1008+7C>T | NP_001305761.1:n.1008+7C>T | |
| NM_001363528.1:c.975+7C>T | NP_001350457.1:n.975+7C>T | |
| NM_021055.2:c.975+7C>T | NP_066399.2:n.975+7C>T | |
| XM_005255531.4:c.975+7C>T | XP_005255588.2:n.975+7C>T | |
| XM_011522636.2:c.975+7C>T | XP_011520938.1:n.975+7C>T | |
| XM_011522637.2:c.975+7C>T | XP_011520939.1:n.975+7C>T | |
| XM_011522638.2:c.1137+7C>T | XP_011520940.2:n.1137+7C>T | |
| XM_011522639.2:c.975+7C>T | XP_011520941.1:n.975+7C>T | |
| XM_011522640.2:c.975+7C>T | XP_011520942.1:n.975+7C>T | |
| XM_017023615.1:c.975+7C>T | XP_016879104.1:n.975+7C>T | |
| XM_017023616.1:c.975+7C>T | XP_016879105.1:n.975+7C>T | |
| XM_017023617.1:c.1137+7C>T | XP_016879106.1:n.1137+7C>T | |
| XM_017023618.1:c.-457+7C>T | XP_016879107.1:n.-457+7C>T | |
| XM_024450413.1:c.975+7C>T | XP_024306181.1:n.975+7C>T | |
| NM_000548.5:c.975+7C>T MANE Select | NP_000539.2:n.975+7C>T | |
| NM_001370404.1:c.975+7C>T | NP_001357333.1:n.975+7C>T | |
| NM_001370405.1:c.975+7C>T | NP_001357334.1:n.975+7C>T | |
| NM_001077183.3:c.975+7C>T | NP_001070651.1:n.975+7C>T | |
| NM_001114382.3:c.975+7C>T | NP_001107854.1:n.975+7C>T | |
| NM_001318827.2:c.864+7C>T | NP_001305756.1:n.864+7C>T | |
| NM_001318829.2:c.828+7C>T | NP_001305758.1:n.828+7C>T | |
| NM_001318831.2:c.375+7C>T | NP_001305760.1:n.375+7C>T | |
| NM_001318832.2:c.1008+7C>T | NP_001305761.1:n.1008+7C>T | |
| NM_001363528.2:c.975+7C>T | NP_001350457.1:n.975+7C>T | |
| NM_021055.3:c.975+7C>T | NP_066399.2:n.975+7C>T |