Linked Data
ClinVar Variation Id:
522237
dbSNP Id:
rs3218620
ExAC:
10:90770373 C / T
gnomAD v2:
10-90770373-C-T
gnomAD v3:
10-89010616-C-T
gnomAD v4:
10-89010616-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.89010616C>T , CM000672.2:g.89010616C>T | GRCh38 |
| NC_000010.10:g.90770373C>T , CM000672.1:g.90770373C>T | GRCh37 |
| NC_000010.9:g.90760353C>T | NCBI36 |
| NG_009089.2:g.25086C>T , LRG_134:g.25086C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313771.10:n.814+16C>T | ||
| ENST00000355740.8:c.505+16C>T | ENSP00000347979.3:n.505+16C>T | |
| ENST00000357339.7:c.505+16C>T | ENSP00000349896.2:n.505+16C>T | |
| ENST00000371857.8:n.731C>T | ||
| ENST00000460510.6:c.-213+16C>T | ENSP00000512812.1:n.-213+16C>T | |
| ENST00000466081.6:n.581C>T | ||
| ENST00000477270.6:c.550+16C>T | ENSP00000512813.1:n.550+16C>T | |
| ENST00000479522.6:c.258+16C>T | ENSP00000424113.1:n.258+16C>T | |
| ENST00000484444.6:c.258+16C>T | ENSP00000420975.1:n.258+16C>T | |
| ENST00000488877.6:c.396+16C>T | ENSP00000425159.1:n.396+16C>T | |
| ENST00000492756.7:c.396+16C>T | ENSP00000422453.1:n.396+16C>T | |
| ENST00000494799.6:c.-213+16C>T | ENSP00000512834.1:n.-213+16C>T | |
| ENST00000562983.3:c.-213+16C>T | ENSP00000512845.1:n.-213+16C>T | |
| ENST00000612663.6:c.505+16C>T | ENSP00000477997.3:n.505+16C>T | |
| ENST00000640140.2:n.650+16C>T | ||
| ENST00000640681.2:n.609+16C>T | ||
| ENST00000696723.1:n.4138+16C>T | ||
| ENST00000696741.1:n.824C>T | ||
| ENST00000696742.1:n.687+16C>T | ||
| ENST00000696743.1:n.693C>T | ||
| ENST00000696744.1:n.544+16C>T | ||
| ENST00000696767.1:n.703C>T | ||
| ENST00000696768.1:c.505+16C>T | ENSP00000512859.1:n.505+16C>T | |
| ENST00000696769.1:n.875C>T | ||
| ENST00000696770.1:n.3296C>T | ||
| ENST00000696771.1:c.-150+16C>T | ENSP00000512860.1:n.-150+16C>T | |
| ENST00000696772.1:n.671+16C>T | ||
| ENST00000696773.1:n.664+16C>T | ||
| ENST00000696774.1:n.2284C>T | ||
| ENST00000696776.1:c.598+16C>T | ENSP00000512861.1:n.598+16C>T | |
| ENST00000696777.1:n.594C>T | ||
| ENST00000696778.1:n.687+16C>T | ||
| ENST00000696779.1:c.258+16C>T | ENSP00000512862.1:n.258+16C>T | |
| ENST00000696780.1:c.598+16C>T | ENSP00000512863.1:n.598+16C>T | |
| ENST00000696781.1:c.396+16C>T | ENSP00000512864.1:n.396+16C>T | |
| ENST00000696782.1:c.505+16C>T | ENSP00000512865.1:n.505+16C>T | |
| ENST00000696783.1:n.1054C>T | ||
| ENST00000696992.1:n.1622+16C>T | ||
| ENST00000696995.1:n.703C>T | ||
| ENST00000696996.1:n.686+16C>T | ||
| ENST00000696997.1:c.*135+16C>T | ENSP00000513028.1:n.*135+16C>T | |
| ENST00000696998.1:n.440C>T | ||
| ENST00000696999.1:c.-150+16C>T | ENSP00000513029.1:n.-150+16C>T | |
| ENST00000697035.1:c.505+16C>T | ENSP00000513059.1:n.505+16C>T | |
| ENST00000697036.1:c.396+16C>T | ENSP00000513060.1:n.396+16C>T | |
| ENST00000697037.1:n.540+16C>T | ||
| ENST00000697093.1:n.729+16C>T | ||
| ENST00000697094.1:n.644+16C>T | ||
| ENST00000697095.1:c.*1706+16C>T | ENSP00000513104.1:n.*1706+16C>T | |
| ENST00000697096.1:n.577C>T | ||
| ENST00000697097.1:c.-213+16C>T | ENSP00000513105.1:n.-213+16C>T | |
| ENST00000562983.2:n.691+16C>T | ||
| ENST00000690268.1:c.586+16C>T | ENSP00000509810.1:n.586+16C>T | |
| ENST00000355740.7:c.505+16C>T | ENSP00000347979.3:n.505+16C>T | |
| ENST00000612663.5:c.505+16C>T | ENSP00000477997.3:n.505+16C>T | |
| ENST00000640140.1:n.677+16C>T | ||
| ENST00000640681.1:n.626+16C>T | ||
| ENST00000652046.1:c.505+16C>T MANE Select | ENSP00000498466.1:n.505+16C>T | |
| ENST00000313771.9:n.814+16C>T | ||
| ENST00000352159.8:c.505+16C>T | ENSP00000345601.4:n.505+16C>T | |
| ENST00000355279.2:c.505+16C>T | ENSP00000347426.2:n.505+16C>T | |
| ENST00000355740.6:c.505+16C>T | ENSP00000347979.2:n.505+16C>T | |
| ENST00000357339.6:c.505+16C>T | ENSP00000349896.2:n.505+16C>T | |
| ENST00000371857.7:n.687C>T | ||
| ENST00000466081.5:n.581C>T | ||
| ENST00000477270.5:n.668+16C>T | ||
| ENST00000479522.5:c.258+16C>T | ENSP00000424113.1:n.258+16C>T | |
| ENST00000484444.5:c.258+16C>T | ENSP00000420975.1:n.258+16C>T | |
| ENST00000487314.1:n.654+16C>T | ||
| ENST00000488877.5:c.396+16C>T | ENSP00000425159.1:n.396+16C>T | |
| ENST00000492756.5:c.396+16C>T | ENSP00000422453.1:n.396+16C>T | |
| ENST00000494410.5:c.396+16C>T | ENSP00000423755.1:n.396+16C>T | |
| ENST00000494799.5:n.412+16C>T | ||
| ENST00000612663.4:c.505+16C>T | ENSP00000477997.2:n.505+16C>T | |
| ENST00000615406.4:c.505+16C>T | ENSP00000484575.1:n.505+16C>T | |
| ENST00000626542.2:c.505+16C>T | ENSP00000485876.1:n.505+16C>T | |
| NM_000043.4:c.505+16C>T , LRG_134t1:c.505+16C>T | NP_000034.1:n.505+16C>T | |
| NM_152871.2:c.505+16C>T | NP_690610.1:n.505+16C>T | |
| NM_152872.2:c.505+16C>T | NP_690611.1:n.505+16C>T | |
| NR_028033.2:n.742+16C>T | ||
| NR_028034.2:n.604+16C>T | ||
| NR_028035.2:n.604+16C>T | ||
| NR_028036.2:n.742+16C>T | ||
| XM_006717819.2:c.586+16C>T | XP_006717882.1:n.586+16C>T | |
| XM_011539764.1:c.667+16C>T | XP_011538066.1:n.667+16C>T | |
| XM_011539765.1:c.667+16C>T | XP_011538067.1:n.667+16C>T | |
| XM_011539766.1:c.586+16C>T | XP_011538068.1:n.586+16C>T | |
| XM_011539767.1:c.550+16C>T | XP_011538069.1:n.550+16C>T | |
| XR_945732.1:n.573+16C>T | ||
| XR_945733.1:n.573+16C>T | ||
| NM_000043.5:c.505+16C>T | NP_000034.1:n.505+16C>T | |
| NM_001320619.1:c.505+16C>T | NP_001307548.1:n.505+16C>T | |
| NM_152871.3:c.505+16C>T | NP_690610.1:n.505+16C>T | |
| NM_152872.3:c.505+16C>T | NP_690611.1:n.505+16C>T | |
| NR_028033.3:n.714+16C>T | ||
| NR_028034.3:n.576+16C>T | ||
| NR_028035.3:n.576+16C>T | ||
| NR_028036.3:n.714+16C>T | ||
| NR_135313.1:n.714+16C>T | ||
| NR_135314.1:n.814+16C>T | ||
| NR_135315.1:n.567+16C>T | ||
| XM_006717819.3:c.586+16C>T | XP_006717882.1:n.586+16C>T | |
| XM_011539764.2:c.667+16C>T | XP_011538066.1:n.667+16C>T | |
| XM_011539765.2:c.667+16C>T | XP_011538067.1:n.667+16C>T | |
| XM_011539766.2:c.586+16C>T | XP_011538068.1:n.586+16C>T | |
| XM_011539767.3:c.550+16C>T | XP_011538069.1:n.550+16C>T | |
| XR_945732.3:n.573+16C>T | ||
| XR_945733.2:n.573+16C>T | ||
| NM_000043.6:c.505+16C>T MANE Select | NP_000034.1:n.505+16C>T | |
| NM_001320619.2:c.505+16C>T | NP_001307548.1:n.505+16C>T | |
| NM_152871.4:c.505+16C>T | NP_690610.1:n.505+16C>T | |
| NM_152872.4:c.505+16C>T | NP_690611.1:n.505+16C>T | |
| NR_028033.4:n.475+16C>T | ||
| NR_028034.4:n.337+16C>T | ||
| NR_028035.4:n.337+16C>T | ||
| NR_028036.4:n.475+16C>T | ||
| NR_135313.2:n.475+16C>T | ||
| NR_135314.2:n.671+16C>T | ||
| NR_135315.2:n.424+16C>T |