Linked Data
ClinVar Variation Id:
286625
dbSNP Id:
rs115640152
ExAC:
8:94770767 C / T
gnomAD v2:
8-94770767-C-T
gnomAD v3:
8-93758539-C-T
gnomAD v4:
8-93758539-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93758539C>T , CM000670.2:g.93758539C>T | GRCh38 |
| NC_000008.10:g.94770767C>T , CM000670.1:g.94770767C>T | GRCh37 |
| NC_000008.9:g.94839943C>T | NCBI36 |
| NG_009190.1:g.8696C>T , LRG_688:g.8696C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.369C>T | ENSP00000314488.4:p.Ala123= | |
| ENST00000409623.8:c.369C>T | ENSP00000386966.4:p.Ala123= | |
| ENST00000452276.6:c.369C>T | ENSP00000388671.2:p.Ala123= | |
| ENST00000453906.6:c.369C>T | ENSP00000403035.2:p.Ala123= | |
| ENST00000520680.2:c.369C>T | ENSP00000428785.2:p.Ala123= | |
| ENST00000521065.2:c.369C>T | ENSP00000427947.2:p.Ala123= | |
| ENST00000521517.6:c.369C>T | ENSP00000430740.2:p.Ala123= | |
| ENST00000681998.1:c.369C>T | ENSP00000506773.1:p.Ala123= | |
| ENST00000682036.1:c.369C>T | ENSP00000508390.1:p.Ala123= | |
| ENST00000682577.1:c.369C>T | ENSP00000506963.1:p.Ala123= | |
| ENST00000682624.1:c.*13C>T | ENSP00000508343.1:n.*13C>T | |
| ENST00000682700.1:c.369C>T | ENSP00000507627.1:p.Ala123= | |
| ENST00000682804.1:n.262C>T | ||
| ENST00000682837.1:c.369C>T | ENSP00000507920.1:p.Ala123= | |
| ENST00000682935.1:n.369C>T | ||
| ENST00000682984.1:c.312+2673C>T | ENSP00000507209.1:n.312+2673C>T | |
| ENST00000683078.1:c.369C>T | ENSP00000506796.1:p.Ala123= | |
| ENST00000683223.1:c.280C>T | ENSP00000507685.1:n.280C>T | |
| ENST00000683238.1:n.190C>T | ||
| ENST00000683249.1:n.390C>T | ||
| ENST00000683336.1:c.369C>T | ENSP00000507695.1:p.Ala123= | |
| ENST00000683362.1:c.312+2673C>T | ENSP00000506985.1:n.312+2673C>T | |
| ENST00000683850.1:n.292C>T | ||
| ENST00000683919.1:c.369C>T | ENSP00000507617.1:p.Ala123= | |
| ENST00000683953.1:c.280C>T | ENSP00000508375.1:n.280C>T | |
| ENST00000684023.1:c.369C>T | ENSP00000507461.1:p.Ala123= | |
| ENST00000684064.1:c.60C>T | ENSP00000508192.1:p.Ala20= | |
| ENST00000684089.1:n.359C>T | ||
| ENST00000684149.1:c.369C>T | ENSP00000507943.1:p.Ala123= | |
| ENST00000684416.1:n.194C>T | ||
| ENST00000684540.1:c.369C>T | ENSP00000507987.1:p.Ala123= | |
| ENST00000684733.1:n.304C>T | ||
| ENST00000453321.8:c.369C>T MANE Select | ENSP00000389998.3:p.Ala123= | |
| ENST00000323130.7:c.339C>T | ENSP00000314488.3:p.Ala113= | |
| ENST00000409623.7:c.-9C>T | ENSP00000386966.3:n.-9C>T | |
| ENST00000452276.5:c.60C>T | ENSP00000388671.1:p.Ala20= | |
| ENST00000453321.7:c.369C>T | ENSP00000389998.3:p.Ala123= | |
| ENST00000453906.5:c.369C>T | ENSP00000403035.1:p.Ala123= | |
| ENST00000455946.5:c.369C>T | ENSP00000416339.1:p.Ala123= | |
| ENST00000474944.5:n.389C>T | ||
| ENST00000475305.1:n.378C>T | ||
| ENST00000498673.5:c.-112C>T | ENSP00000430232.1:n.-112C>T | |
| ENST00000518319.5:c.-151C>T | ENSP00000430289.1:n.-151C>T | |
| ENST00000521065.1:c.275C>T | ||
| ENST00000521222.5:c.*5C>T | ENSP00000429925.1:n.*5C>T | |
| ENST00000521517.5:c.361C>T | ||
| NM_001142301.1:c.-9C>T , LRG_688t2:c.-9C>T | NP_001135773.1:n.-9C>T | |
| NM_153704.5:c.369C>T , LRG_688t1:c.369C>T | NP_714915.3:p.Ala123= | |
| NR_024522.1:n.440C>T | ||
| XM_006716686.2:c.66C>T | XP_006716749.1:p.Ala22= | |
| XM_011517363.1:c.369C>T | XP_011515665.1:p.Ala123= | |
| XR_428387.1:n.427C>T | ||
| XR_928360.1:n.427C>T | ||
| XR_928361.1:n.427C>T | ||
| XR_928362.1:n.427C>T | ||
| XM_006716686.4:c.66C>T | XP_006716749.1:p.Ala22= | |
| XM_011517363.3:c.369C>T | XP_011515665.1:p.Ala123= | |
| XM_024447326.1:c.-41C>T | XP_024303094.1:n.-41C>T | |
| XR_001745619.2:n.410C>T | ||
| XR_428387.2:n.410C>T | ||
| XR_928360.3:n.410C>T | ||
| XR_928362.3:n.410C>T | ||
| NM_153704.6:c.369C>T MANE Select | NP_714915.3:p.Ala123= | |
| NR_024522.2:n.390C>T |