Linked Data
ClinVar Variation Id:
1291169
ClinVar RCV Id:
RCV001713192
dbSNP Id:
rs2296603
gnomAD v2:
10-90763127-C-T
gnomAD v3:
10-89003370-C-T
gnomAD v4:
10-89003370-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.89003370C>T , CM000672.2:g.89003370C>T | GRCh38 |
| NC_000010.10:g.90763127C>T , CM000672.1:g.90763127C>T | GRCh37 |
| NC_000010.9:g.90753107C>T | NCBI36 |
| NG_009089.2:g.17840C>T , LRG_134:g.17840C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000313771.10:n.505+176C>T | ||
| ENST00000355740.8:c.196+176C>T | ENSP00000347979.3:n.196+176C>T | |
| ENST00000357339.7:c.196+176C>T | ENSP00000349896.2:n.196+176C>T | |
| ENST00000371857.8:n.406+176C>T | ||
| ENST00000460510.6:c.-522+176C>T | ENSP00000512812.1:n.-522+176C>T | |
| ENST00000466081.6:n.365+176C>T | ||
| ENST00000477270.6:c.241+176C>T | ENSP00000512813.1:n.241+176C>T | |
| ENST00000479522.6:c.196+176C>T | ENSP00000424113.1:n.196+176C>T | |
| ENST00000484444.6:c.196+176C>T | ENSP00000420975.1:n.196+176C>T | |
| ENST00000488877.6:c.196+176C>T | ENSP00000425159.1:n.196+176C>T | |
| ENST00000492756.7:c.196+176C>T | ENSP00000422453.1:n.196+176C>T | |
| ENST00000494799.6:c.-275+176C>T | ENSP00000512834.1:n.-275+176C>T | |
| ENST00000562983.3:c.-522+176C>T | ENSP00000512845.1:n.-522+176C>T | |
| ENST00000612663.6:c.196+176C>T | ENSP00000477997.3:n.196+176C>T | |
| ENST00000640140.2:n.341+176C>T | ||
| ENST00000640681.2:n.300+176C>T | ||
| ENST00000696723.1:n.3829+176C>T | ||
| ENST00000696741.1:n.499+176C>T | ||
| ENST00000696742.1:n.378+176C>T | ||
| ENST00000696743.1:n.368+176C>T | ||
| ENST00000696744.1:n.235+176C>T | ||
| ENST00000696767.1:n.378+176C>T | ||
| ENST00000696768.1:c.196+176C>T | ENSP00000512859.1:n.196+176C>T | |
| ENST00000696769.1:n.550+176C>T | ||
| ENST00000696770.1:n.379+176C>T | ||
| ENST00000696771.1:c.-459+176C>T | ENSP00000512860.1:n.-459+176C>T | |
| ENST00000696772.1:n.362+176C>T | ||
| ENST00000696773.1:n.355+176C>T | ||
| ENST00000696774.1:n.418+176C>T | ||
| ENST00000696775.1:n.471+176C>T | ||
| ENST00000696776.1:c.289+176C>T | ENSP00000512861.1:n.289+176C>T | |
| ENST00000696777.1:n.378+176C>T | ||
| ENST00000696778.1:n.378+176C>T | ||
| ENST00000696779.1:c.196+176C>T | ENSP00000512862.1:n.196+176C>T | |
| ENST00000696780.1:c.289+176C>T | ENSP00000512863.1:n.289+176C>T | |
| ENST00000696781.1:c.196+176C>T | ENSP00000512864.1:n.196+176C>T | |
| ENST00000696782.1:c.196+176C>T | ENSP00000512865.1:n.196+176C>T | |
| ENST00000696992.1:n.1313+176C>T | ||
| ENST00000696994.1:n.378+176C>T | ||
| ENST00000696995.1:n.378+176C>T | ||
| ENST00000696996.1:n.377+176C>T | ||
| ENST00000696997.1:c.196+176C>T | ENSP00000513028.1:n.196+176C>T | |
| ENST00000696998.1:n.362+176C>T | ||
| ENST00000696999.1:c.-350+176C>T | ENSP00000513029.1:n.-350+176C>T | |
| ENST00000697035.1:c.196+176C>T | ENSP00000513059.1:n.196+176C>T | |
| ENST00000697036.1:c.196+176C>T | ENSP00000513060.1:n.196+176C>T | |
| ENST00000697037.1:n.231+176C>T | ||
| ENST00000697093.1:n.420+176C>T | ||
| ENST00000697094.1:n.335+176C>T | ||
| ENST00000697095.1:c.196+176C>T | ENSP00000513104.1:n.196+176C>T | |
| ENST00000697096.1:n.252+176C>T | ||
| ENST00000697097.1:c.-522+176C>T | ENSP00000513105.1:n.-522+176C>T | |
| ENST00000562983.2:n.382+176C>T | ||
| ENST00000690268.1:c.277+176C>T | ENSP00000509810.1:n.277+176C>T | |
| ENST00000355740.7:c.196+176C>T | ENSP00000347979.3:n.196+176C>T | |
| ENST00000612663.5:c.196+176C>T | ENSP00000477997.3:n.196+176C>T | |
| ENST00000640140.1:n.368+176C>T | ||
| ENST00000640681.1:n.317+176C>T | ||
| ENST00000652046.1:c.196+176C>T MANE Select | ENSP00000498466.1:n.196+176C>T | |
| ENST00000313771.9:n.505+176C>T | ||
| ENST00000352159.8:c.196+176C>T | ENSP00000345601.4:n.196+176C>T | |
| ENST00000355279.2:c.196+176C>T | ENSP00000347426.2:n.196+176C>T | |
| ENST00000355740.6:c.196+176C>T | ENSP00000347979.2:n.196+176C>T | |
| ENST00000357339.6:c.196+176C>T | ENSP00000349896.2:n.196+176C>T | |
| ENST00000371857.7:n.362+176C>T | ||
| ENST00000460510.5:n.563+176C>T | ||
| ENST00000466081.5:n.365+176C>T | ||
| ENST00000477270.5:n.359+176C>T | ||
| ENST00000479522.5:c.196+176C>T | ENSP00000424113.1:n.196+176C>T | |
| ENST00000484444.5:c.196+176C>T | ENSP00000420975.1:n.196+176C>T | |
| ENST00000487314.1:n.345+176C>T | ||
| ENST00000488877.5:c.196+176C>T | ENSP00000425159.1:n.196+176C>T | |
| ENST00000492756.5:c.196+176C>T | ENSP00000422453.1:n.196+176C>T | |
| ENST00000494410.5:c.196+176C>T | ENSP00000423755.1:n.196+176C>T | |
| ENST00000494799.5:n.350+176C>T | ||
| ENST00000612663.4:c.196+176C>T | ENSP00000477997.2:n.196+176C>T | |
| ENST00000615406.4:c.196+176C>T | ENSP00000484575.1:n.196+176C>T | |
| ENST00000626542.2:c.196+176C>T | ENSP00000485876.1:n.196+176C>T | |
| NM_000043.4:c.196+176C>T , LRG_134t1:c.196+176C>T | NP_000034.1:n.196+176C>T | |
| NM_152871.2:c.196+176C>T | NP_690610.1:n.196+176C>T | |
| NM_152872.2:c.196+176C>T | NP_690611.1:n.196+176C>T | |
| NR_028033.2:n.542+176C>T | ||
| NR_028034.2:n.542+176C>T | ||
| NR_028035.2:n.542+176C>T | ||
| NR_028036.2:n.542+176C>T | ||
| XM_006717819.2:c.277+176C>T | XP_006717882.1:n.277+176C>T | |
| XM_011539764.1:c.358+176C>T | XP_011538066.1:n.358+176C>T | |
| XM_011539765.1:c.358+176C>T | XP_011538067.1:n.358+176C>T | |
| XM_011539766.1:c.277+176C>T | XP_011538068.1:n.277+176C>T | |
| XM_011539767.1:c.241+176C>T | XP_011538069.1:n.241+176C>T | |
| XR_945732.1:n.373+176C>T | ||
| XR_945733.1:n.373+176C>T | ||
| NM_000043.5:c.196+176C>T | NP_000034.1:n.196+176C>T | |
| NM_001320619.1:c.196+176C>T | NP_001307548.1:n.196+176C>T | |
| NM_152871.3:c.196+176C>T | NP_690610.1:n.196+176C>T | |
| NM_152872.3:c.196+176C>T | NP_690611.1:n.196+176C>T | |
| NR_028033.3:n.514+176C>T | ||
| NR_028034.3:n.514+176C>T | ||
| NR_028035.3:n.514+176C>T | ||
| NR_028036.3:n.514+176C>T | ||
| NR_135313.1:n.514+176C>T | ||
| NR_135314.1:n.505+176C>T | ||
| NR_135315.1:n.505+176C>T | ||
| XM_006717819.3:c.277+176C>T | XP_006717882.1:n.277+176C>T | |
| XM_011539764.2:c.358+176C>T | XP_011538066.1:n.358+176C>T | |
| XM_011539765.2:c.358+176C>T | XP_011538067.1:n.358+176C>T | |
| XM_011539766.2:c.277+176C>T | XP_011538068.1:n.277+176C>T | |
| XM_011539767.3:c.241+176C>T | XP_011538069.1:n.241+176C>T | |
| XR_945732.3:n.373+176C>T | ||
| XR_945733.2:n.373+176C>T | ||
| NM_000043.6:c.196+176C>T MANE Select | NP_000034.1:n.196+176C>T | |
| NM_001320619.2:c.196+176C>T | NP_001307548.1:n.196+176C>T | |
| NM_152871.4:c.196+176C>T | NP_690610.1:n.196+176C>T | |
| NM_152872.4:c.196+176C>T | NP_690611.1:n.196+176C>T | |
| NR_028033.4:n.275+176C>T | ||
| NR_028034.4:n.275+176C>T | ||
| NR_028035.4:n.275+176C>T | ||
| NR_028036.4:n.275+176C>T | ||
| NR_135313.2:n.275+176C>T | ||
| NR_135314.2:n.362+176C>T | ||
| NR_135315.2:n.362+176C>T |