Linked Data
dbSNP Id:
rs1320026119
gnomAD v2:
8-94777598-T-G
gnomAD v3:
8-93765370-T-G
gnomAD v4:
8-93765370-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93765370T>G , CM000670.2:g.93765370T>G | GRCh38 |
| NC_000008.10:g.94777598T>G , CM000670.1:g.94777598T>G | GRCh37 |
| NC_000008.9:g.94846774T>G | NCBI36 |
| NG_009190.1:g.15527T>G , LRG_688:g.15527T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.507-36T>G | ENSP00000314488.4:n.507-36T>G | |
| ENST00000409623.8:c.507-36T>G | ENSP00000386966.4:n.507-36T>G | |
| ENST00000452276.6:c.507-36T>G | ENSP00000388671.2:n.507-36T>G | |
| ENST00000453906.6:c.406+6794T>G | ENSP00000403035.2:n.406+6794T>G | |
| ENST00000520680.2:c.507-36T>G | ENSP00000428785.2:n.507-36T>G | |
| ENST00000521065.2:c.*224-36T>G | ENSP00000427947.2:n.*224-36T>G | |
| ENST00000521517.6:c.507-36T>G | ENSP00000430740.2:n.507-36T>G | |
| ENST00000681998.1:c.507-202T>G | ENSP00000506773.1:n.507-202T>G | |
| ENST00000682036.1:c.406+6794T>G | ENSP00000508390.1:n.406+6794T>G | |
| ENST00000682577.1:c.507-202T>G | ENSP00000506963.1:n.507-202T>G | |
| ENST00000682624.1:c.*151-202T>G | ENSP00000508343.1:n.*151-202T>G | |
| ENST00000682700.1:c.507-36T>G | ENSP00000507627.1:n.507-36T>G | |
| ENST00000682804.1:n.400-202T>G | ||
| ENST00000682837.1:c.406+6794T>G | ENSP00000507920.1:n.406+6794T>G | |
| ENST00000682935.1:n.1935T>G | ||
| ENST00000682984.1:c.313-7219T>G | ENSP00000507209.1:n.313-7219T>G | |
| ENST00000683078.1:c.406+6794T>G | ENSP00000506796.1:n.406+6794T>G | |
| ENST00000683223.1:c.418-202T>G | ENSP00000507685.1:n.418-202T>G | |
| ENST00000683238.1:n.1756T>G | ||
| ENST00000683249.1:n.1956T>G | ||
| ENST00000683336.1:c.507-202T>G | ENSP00000507695.1:n.507-202T>G | |
| ENST00000683362.1:c.313-7219T>G | ENSP00000506985.1:n.313-7219T>G | |
| ENST00000683850.1:n.430-36T>G | ||
| ENST00000683919.1:c.507-202T>G | ENSP00000507617.1:n.507-202T>G | |
| ENST00000683953.1:c.418-36T>G | ENSP00000508375.1:n.418-36T>G | |
| ENST00000684023.1:c.641-36T>G | ENSP00000507461.1:n.641-36T>G | |
| ENST00000684064.1:c.198-36T>G | ENSP00000508192.1:n.198-36T>G | |
| ENST00000684089.1:n.1925T>G | ||
| ENST00000684149.1:c.507-202T>G | ENSP00000507943.1:n.507-202T>G | |
| ENST00000684416.1:n.466-36T>G | ||
| ENST00000684540.1:c.507-202T>G | ENSP00000507987.1:n.507-202T>G | |
| ENST00000453321.8:c.507-36T>G MANE Select | ENSP00000389998.3:n.507-36T>G | |
| ENST00000323130.7:c.477-36T>G | ENSP00000314488.3:n.477-36T>G | |
| ENST00000409623.7:c.264-36T>G | ENSP00000386966.3:n.264-36T>G | |
| ENST00000452276.5:c.198-36T>G | ENSP00000388671.1:n.198-36T>G | |
| ENST00000453321.7:c.507-36T>G | ENSP00000389998.3:n.507-36T>G | |
| ENST00000453906.5:c.406+6794T>G | ENSP00000403035.1:n.406+6794T>G | |
| ENST00000455946.5:c.*179-36T>G | ENSP00000416339.1:n.*179-36T>G | |
| ENST00000474944.5:n.426+6794T>G | ||
| ENST00000518319.5:c.27-36T>G | ENSP00000430289.1:n.27-36T>G | |
| ENST00000521065.1:c.413-36T>G | ||
| ENST00000521222.5:c.*143-36T>G | ENSP00000429925.1:n.*143-36T>G | |
| ENST00000521517.5:c.499-202T>G | ||
| NM_001142301.1:c.264-36T>G , LRG_688t2:c.264-36T>G | NP_001135773.1:n.264-36T>G | |
| NM_153704.5:c.507-36T>G , LRG_688t1:c.507-36T>G | NP_714915.3:n.507-36T>G | |
| NR_024522.1:n.578-36T>G | ||
| XM_006716686.2:c.204-36T>G | XP_006716749.1:n.204-36T>G | |
| XM_011517363.1:c.406+6794T>G | XP_011515665.1:n.406+6794T>G | |
| XR_428387.1:n.565-36T>G | ||
| XR_928360.1:n.565-36T>G | ||
| XR_928361.1:n.565-36T>G | ||
| XR_928362.1:n.565-36T>G | ||
| XM_006716686.4:c.204-36T>G | XP_006716749.1:n.204-36T>G | |
| XM_011517363.3:c.406+6794T>G | XP_011515665.1:n.406+6794T>G | |
| XM_024447326.1:c.-4+6794T>G | XP_024303094.1:n.-4+6794T>G | |
| XR_001745619.2:n.548-36T>G | ||
| XR_428387.2:n.548-36T>G | ||
| XR_928360.3:n.548-36T>G | ||
| XR_928362.3:n.548-36T>G | ||
| NM_153704.6:c.507-36T>G MANE Select | NP_714915.3:n.507-36T>G | |
| NR_024522.2:n.528-36T>G |