Linked Data
ClinVar Variation Id:
160096
dbSNP Id:
rs76843552
ExAC:
12:111052219 G / C
gnomAD v2:
12-111052219-G-C
gnomAD v3:
12-110614414-G-C
gnomAD v4:
12-110614414-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110614414G>C , CM000674.2:g.110614414G>C | GRCh38 |
| NC_000012.11:g.111052219G>C , CM000674.1:g.111052219G>C | GRCh37 |
| NC_000012.10:g.109536602G>C | NCBI36 |
| NG_030381.1:g.5388G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377654.5:c.220+12G>C | ENSP00000366882.5:n.220+12G>C | |
| ENST00000397659.9:c.220+12G>C MANE Select | ENSP00000380779.4:n.220+12G>C | |
| ENST00000471804.7:c.220+12G>C | ENSP00000473903.2:n.220+12G>C | |
| ENST00000547461.3:c.220+12G>C | ENSP00000448188.3:n.220+12G>C | |
| ENST00000549123.6:c.220+12G>C | ENSP00000450154.2:n.220+12G>C | |
| ENST00000551555.3:n.273+12G>C | ||
| ENST00000552038.6:n.290+12G>C | ||
| ENST00000614115.5:c.220+12G>C | ENSP00000484255.2:n.220+12G>C | |
| ENST00000679401.1:c.232G>C | ENSP00000506277.1:p.Val78Leu | |
| ENST00000679473.1:c.220+12G>C | ENSP00000504983.1:n.220+12G>C | |
| ENST00000679617.1:c.220+12G>C | ENSP00000506626.1:n.220+12G>C | |
| ENST00000679713.1:c.220+12G>C | ENSP00000504975.1:n.220+12G>C | |
| ENST00000680068.1:c.220+12G>C | ENSP00000506300.1:n.220+12G>C | |
| ENST00000680203.1:c.220+12G>C | ENSP00000505195.1:n.220+12G>C | |
| ENST00000680445.1:c.220+12G>C | ENSP00000505462.1:n.220+12G>C | |
| ENST00000680512.1:c.220+12G>C | ENSP00000505935.1:n.220+12G>C | |
| ENST00000680548.1:c.220+12G>C | ENSP00000505310.1:n.220+12G>C | |
| ENST00000680571.1:n.266+12G>C | ||
| ENST00000681395.1:c.220+12G>C | ENSP00000505886.1:n.220+12G>C | |
| ENST00000681437.1:c.220+12G>C | ENSP00000505004.1:n.220+12G>C | |
| ENST00000681604.1:c.220+12G>C | ENSP00000505920.1:n.220+12G>C | |
| ENST00000681740.1:n.266+12G>C | ||
| ENST00000681807.1:c.220+12G>C | ENSP00000505236.1:n.220+12G>C | |
| ENST00000681851.1:c.220+12G>C | ENSP00000505956.1:n.220+12G>C | |
| ENST00000397655.7:c.220+12G>C | ENSP00000380775.3:n.220+12G>C | |
| ENST00000397656.8:c.220+12G>C | ENSP00000380776.4:n.220+12G>C | |
| ENST00000397659.8:c.220+12G>C | ENSP00000380779.4:n.220+12G>C | |
| ENST00000464809.5:c.232G>C | ENSP00000435027.1:p.Val78Leu | |
| ENST00000471804.6:c.220+12G>C | ENSP00000473903.1:n.220+12G>C | |
| ENST00000478122.6:c.232G>C | ENSP00000474208.1:p.Val78Leu | |
| ENST00000480648.5:c.220+12G>C | ENSP00000437196.1:n.220+12G>C | |
| ENST00000481720.5:c.220+12G>C | ENSP00000474291.1:n.220+12G>C | |
| ENST00000490514.5:c.220+12G>C | ENSP00000436044.1:n.220+12G>C | |
| ENST00000495659.6:c.232G>C | ENSP00000436673.2:p.Val78Leu | |
| ENST00000498072.5:c.220+12G>C | ENSP00000474525.1:n.220+12G>C | |
| ENST00000546643.1:c.220+12G>C | ENSP00000473743.1:n.220+12G>C | |
| ENST00000547868.1:n.264+12G>C | ||
| ENST00000550703.6:c.220+12G>C | ENSP00000473789.1:n.220+12G>C | |
| ENST00000551590.5:c.220+12G>C | ENSP00000448735.1:n.220+12G>C | |
| ENST00000552318.5:c.220+12G>C | ENSP00000474343.1:n.220+12G>C | |
| ENST00000614115.4:c.220+12G>C | ENSP00000484255.1:n.220+12G>C | |
| NM_001082537.2:c.220+12G>C | NP_001076006.1:n.220+12G>C | |
| NM_001082538.2:c.220+12G>C | NP_001076007.1:n.220+12G>C | |
| NM_001173975.1:c.3G>C | NP_001167446.1:p.Met1Ile | |
| NM_001173976.1:c.-37+12G>C | NP_001167447.1:n.-37+12G>C | |
| NM_024549.5:c.220+12G>C | NP_078825.2:n.220+12G>C | |
| XM_005253934.2:c.220+12G>C | XP_005253991.1:n.220+12G>C | |
| XM_005253935.2:c.220+12G>C | XP_005253992.1:n.220+12G>C | |
| XM_005253936.2:c.-488+12G>C | XP_005253993.1:n.-488+12G>C | |
| XM_006719594.1:c.3G>C | XP_006719657.1:p.Met1Ile | |
| XM_006719595.1:c.-472+12G>C | XP_006719658.1:n.-472+12G>C | |
| XM_006719596.1:c.-488+12G>C | XP_006719659.1:n.-488+12G>C | |
| XM_006719597.2:c.-194+12G>C | XP_006719660.1:n.-194+12G>C | |
| XM_006719598.1:c.-458+12G>C | XP_006719661.1:n.-458+12G>C | |
| XM_006719599.1:c.-285+12G>C | XP_006719662.1:n.-285+12G>C | |
| XM_006719600.1:c.-164+12G>C | XP_006719663.1:n.-164+12G>C | |
| XM_011538733.1:c.220+12G>C | XP_011537035.1:n.220+12G>C | |
| XM_011538734.1:c.232G>C | XP_011537036.1:p.Val78Leu | |
| XM_011538735.1:c.220+12G>C | XP_011537037.1:n.220+12G>C | |
| XM_011538736.1:c.220+12G>C | XP_011537038.1:n.220+12G>C | |
| XM_011538737.1:c.220+12G>C | XP_011537039.1:n.220+12G>C | |
| XM_011538738.1:c.220+12G>C | XP_011537040.1:n.220+12G>C | |
| XM_011538739.1:c.220+12G>C | XP_011537041.1:n.220+12G>C | |
| XR_243021.2:n.280+12G>C | ||
| XR_243022.2:n.280+12G>C | ||
| XR_429116.1:n.280+12G>C | ||
| XR_944717.1:n.280+12G>C | ||
| NM_001173975.2:c.3G>C | NP_001167446.1:p.Met1Ile | |
| NM_001319680.1:c.220+12G>C | NP_001306609.1:n.220+12G>C | |
| NM_001319681.1:c.-488+12G>C | NP_001306610.1:n.-488+12G>C | |
| NM_001319682.1:c.3G>C | NP_001306611.1:p.Met1Ile | |
| NR_135088.1:n.388G>C | ||
| XM_005253934.4:c.220+12G>C | XP_005253991.1:n.220+12G>C | |
| XM_005253935.4:c.220+12G>C | XP_005253992.1:n.220+12G>C | |
| XM_006719594.3:c.3G>C | XP_006719657.1:p.Met1Ile | |
| XM_006719595.3:c.-472+12G>C | XP_006719658.1:n.-472+12G>C | |
| XM_006719596.3:c.-488+12G>C | XP_006719659.1:n.-488+12G>C | |
| XM_006719597.4:c.-194+12G>C | XP_006719660.1:n.-194+12G>C | |
| XM_006719598.3:c.-458+12G>C | XP_006719661.1:n.-458+12G>C | |
| XM_006719599.3:c.-285+12G>C | XP_006719662.1:n.-285+12G>C | |
| XM_006719600.3:c.-164+12G>C | XP_006719663.1:n.-164+12G>C | |
| XM_011538733.3:c.220+12G>C | XP_011537035.1:n.220+12G>C | |
| XM_011538734.3:c.232G>C | XP_011537036.1:p.Val78Leu | |
| XM_011538735.2:c.220+12G>C | XP_011537037.1:n.220+12G>C | |
| XM_011538737.3:c.220+12G>C | XP_011537039.1:n.220+12G>C | |
| XM_011538738.3:c.220+12G>C | XP_011537040.1:n.220+12G>C | |
| XM_017019964.1:c.3G>C | XP_016875453.1:p.Met1Ile | |
| XM_017019966.2:c.-659G>C | XP_016875455.1:n.-659G>C | |
| XM_017019968.2:c.-367+12G>C | XP_016875457.1:n.-367+12G>C | |
| XM_017019969.2:c.-285+12G>C | XP_016875458.1:n.-285+12G>C | |
| XR_243021.4:n.274+12G>C | ||
| XR_243022.4:n.274+12G>C | ||
| XR_429116.3:n.274+12G>C | ||
| XR_944717.3:n.274+12G>C | ||
| NM_001082537.3:c.220+12G>C | NP_001076006.1:n.220+12G>C | |
| NM_001082538.3:c.220+12G>C MANE Select | NP_001076007.1:n.220+12G>C | |
| NM_001173975.3:c.3G>C | NP_001167446.1:p.Met1Ile | |
| NM_001173976.2:c.-37+12G>C | NP_001167447.1:n.-37+12G>C | |
| NM_001319680.2:c.220+12G>C | NP_001306609.1:n.220+12G>C | |
| NM_001319681.2:c.-488+12G>C | NP_001306610.1:n.-488+12G>C | |
| NM_001319682.2:c.3G>C | NP_001306611.1:p.Met1Ile | |
| NM_024549.6:c.220+12G>C | NP_078825.2:n.220+12G>C | |
| NR_135088.2:n.286G>C | ||
| NM_001319682.3:c.3G>C | NP_001306611.1:p.Met1Ile |