Linked Data
ClinVar Variation Id:
413725
dbSNP Id:
rs747827911
ExAC:
16:2137950 C / T
gnomAD v2:
16-2137950-C-T
gnomAD v3:
16-2087949-C-T
gnomAD v4:
16-2087949-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2087949C>T , CM000678.2:g.2087949C>T | GRCh38 |
| NC_000016.9:g.2137950C>T , CM000678.1:g.2137950C>T | GRCh37 |
| NC_000016.8:g.2077951C>T | NCBI36 |
| NG_005895.1:g.43644C>T , LRG_487:g.43644C>T | |
| NG_008617.1:g.55272G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*3417+8C>T | ENSP00000455997.2:n.*3417+8C>T | |
| ENST00000642206.2:c.4915+8C>T | ENSP00000495146.2:n.4915+8C>T | |
| ENST00000642365.2:c.5065+8C>T | ENSP00000495459.2:n.5065+8C>T | |
| ENST00000644417.2:c.*5581+8C>T | ENSP00000493912.2:n.*5581+8C>T | |
| ENST00000646464.2:c.*7817+8C>T | ENSP00000496610.2:n.*7817+8C>T | |
| ENST00000219476.9:c.5068+8C>T MANE Select | ENSP00000219476.3:n.5068+8C>T | |
| ENST00000350773.9:c.4999+8C>T | ENSP00000344383.4:n.4999+8C>T | |
| ENST00000401874.7:c.4867+8C>T | ENSP00000384468.2:n.4867+8C>T | |
| ENST00000568454.6:c.4900+8C>T | ENSP00000454487.1:n.4900+8C>T | |
| ENST00000569110.2:c.1291+8C>T | ||
| ENST00000569930.2:n.2950+8C>T | ||
| ENST00000642365.1:c.3722+8C>T | ||
| ENST00000642561.1:c.4939+8C>T | ENSP00000495099.1:n.4939+8C>T | |
| ENST00000642791.1:n.665+8C>T | ||
| ENST00000642797.1:c.4870+8C>T | ENSP00000493846.1:n.4870+8C>T | |
| ENST00000642936.1:c.4936+8C>T | ENSP00000494514.1:n.4936+8C>T | |
| ENST00000643088.1:c.4861+8C>T | ENSP00000494747.1:n.4861+8C>T | |
| ENST00000643177.1:n.1090C>T | ||
| ENST00000643426.1:n.2716+8C>T | ||
| ENST00000643946.1:c.4993+8C>T | ENSP00000495927.1:n.4993+8C>T | |
| ENST00000644043.1:c.4939+8C>T | ENSP00000496262.1:n.4939+8C>T | |
| ENST00000644278.1:n.558C>T | ||
| ENST00000644329.1:c.4867+8C>T | ENSP00000496611.1:n.4867+8C>T | |
| ENST00000644335.1:c.4864+8C>T | ENSP00000496317.1:n.4864+8C>T | |
| ENST00000644399.1:c.4989+8C>T | ||
| ENST00000645024.1:n.3152+8C>T | ||
| ENST00000646388.1:c.5062+8C>T | ENSP00000495921.1:n.5062+8C>T | |
| ENST00000646634.1:n.3883+8C>T | ||
| ENST00000646674.1:n.2320+8C>T | ||
| ENST00000647042.1:n.2291+8C>T | ||
| ENST00000647180.1:n.2181+8C>T | ||
| ENST00000219476.7:c.5068+8C>T | ENSP00000219476.3:n.5068+8C>T | |
| ENST00000350773.8:c.4999+8C>T | ENSP00000344383.4:n.4999+8C>T | |
| ENST00000382538.10:c.4723+8C>T | ENSP00000371978.6:n.4723+8C>T | |
| ENST00000401874.6:c.4867+8C>T | ENSP00000384468.2:n.4867+8C>T | |
| ENST00000439117.6:c.*4235+8C>T | ENSP00000406980.2:n.*4235+8C>T | |
| ENST00000439673.6:c.4759+8C>T | ENSP00000399232.2:n.4759+8C>T | |
| ENST00000497886.5:n.2791+8C>T | ||
| ENST00000568454.5:c.4900+8C>T | ENSP00000454487.1:n.4900+8C>T | |
| ENST00000569110.1:c.1250+8C>T | ||
| ENST00000569930.1:n.2183+8C>T | ||
| NM_000548.3:c.5068+8C>T , LRG_487t1:c.5068+8C>T | NP_000539.2:n.5068+8C>T | |
| NM_001077183.1:c.4867+8C>T | NP_001070651.1:n.4867+8C>T | |
| NM_001114382.1:c.4999+8C>T | NP_001107854.1:n.4999+8C>T | |
| XM_005255529.3:c.4939+8C>T | XP_005255586.2:n.4939+8C>T | |
| XM_005255531.3:c.4870+8C>T | XP_005255588.2:n.4870+8C>T | |
| XM_011522636.1:c.5122+8C>T | XP_011520938.1:n.5122+8C>T | |
| XM_011522637.1:c.5119+8C>T | XP_011520939.1:n.5119+8C>T | |
| XM_011522638.1:c.5011+8C>T | XP_011520940.1:n.5011+8C>T | |
| XM_011522639.1:c.4993+8C>T | XP_011520941.1:n.4993+8C>T | |
| XM_011522640.1:c.4990+8C>T | XP_011520942.1:n.4990+8C>T | |
| XM_011522641.1:c.4759+8C>T | XP_011520943.1:n.4759+8C>T | |
| NM_000548.4:c.5068+8C>T | NP_000539.2:n.5068+8C>T | |
| NM_001077183.2:c.4867+8C>T | NP_001070651.1:n.4867+8C>T | |
| NM_001114382.2:c.4999+8C>T | NP_001107854.1:n.4999+8C>T | |
| NM_001318827.1:c.4759+8C>T | NP_001305756.1:n.4759+8C>T | |
| NM_001318829.1:c.4723+8C>T | NP_001305758.1:n.4723+8C>T | |
| NM_001318831.1:c.4336+8C>T | NP_001305760.1:n.4336+8C>T | |
| NM_001318832.1:c.4900+8C>T | NP_001305761.1:n.4900+8C>T | |
| NM_001363528.1:c.4870+8C>T | NP_001350457.1:n.4870+8C>T | |
| NM_021055.2:c.4939+8C>T | NP_066399.2:n.4939+8C>T | |
| XM_005255531.4:c.4870+8C>T | XP_005255588.2:n.4870+8C>T | |
| XM_011522636.2:c.5122+8C>T | XP_011520938.1:n.5122+8C>T | |
| XM_011522637.2:c.5119+8C>T | XP_011520939.1:n.5119+8C>T | |
| XM_011522638.2:c.5284+8C>T | XP_011520940.2:n.5284+8C>T | |
| XM_011522639.2:c.4993+8C>T | XP_011520941.1:n.4993+8C>T | |
| XM_011522640.2:c.4990+8C>T | XP_011520942.1:n.4990+8C>T | |
| XM_017023615.1:c.5065+8C>T | XP_016879104.1:n.5065+8C>T | |
| XM_017023616.1:c.4936+8C>T | XP_016879105.1:n.4936+8C>T | |
| XM_017023617.1:c.5032+8C>T | XP_016879106.1:n.5032+8C>T | |
| XM_017023618.1:c.3778+8C>T | XP_016879107.1:n.3778+8C>T | |
| XM_024450413.1:c.4867+8C>T | XP_024306181.1:n.4867+8C>T | |
| NM_000548.5:c.5068+8C>T MANE Select | NP_000539.2:n.5068+8C>T | |
| NM_001370404.1:c.4936+8C>T | NP_001357333.1:n.4936+8C>T | |
| NM_001370405.1:c.4939+8C>T | NP_001357334.1:n.4939+8C>T | |
| NM_001077183.3:c.4867+8C>T | NP_001070651.1:n.4867+8C>T | |
| NM_001114382.3:c.4999+8C>T | NP_001107854.1:n.4999+8C>T | |
| NM_001318827.2:c.4759+8C>T | NP_001305756.1:n.4759+8C>T | |
| NM_001318829.2:c.4723+8C>T | NP_001305758.1:n.4723+8C>T | |
| NM_001318831.2:c.4336+8C>T | NP_001305760.1:n.4336+8C>T | |
| NM_001318832.2:c.4900+8C>T | NP_001305761.1:n.4900+8C>T | |
| NM_001363528.2:c.4870+8C>T | NP_001350457.1:n.4870+8C>T | |
| NM_021055.3:c.4939+8C>T | NP_066399.2:n.4939+8C>T |