Linked Data
ClinVar Variation Id:
2929937
ClinVar RCV Id:
RCV003787295
dbSNP Id:
rs1291015693
gnomAD v2:
8-94770788-C-T
gnomAD v3:
8-93758560-C-T
gnomAD v4:
8-93758560-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93758560C>T , CM000670.2:g.93758560C>T | GRCh38 |
| NC_000008.10:g.94770788C>T , CM000670.1:g.94770788C>T | GRCh37 |
| NC_000008.9:g.94839964C>T | NCBI36 |
| NG_009190.1:g.8717C>T , LRG_688:g.8717C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.390C>T | ENSP00000314488.4:p.Pro130= | |
| ENST00000409623.8:c.390C>T | ENSP00000386966.4:p.Pro130= | |
| ENST00000452276.6:c.390C>T | ENSP00000388671.2:p.Pro130= | |
| ENST00000453906.6:c.390C>T | ENSP00000403035.2:p.Pro130= | |
| ENST00000520680.2:c.390C>T | ENSP00000428785.2:p.Pro130= | |
| ENST00000521065.2:c.390C>T | ENSP00000427947.2:p.Pro130= | |
| ENST00000521517.6:c.390C>T | ENSP00000430740.2:p.Pro130= | |
| ENST00000681998.1:c.390C>T | ENSP00000506773.1:p.Pro130= | |
| ENST00000682036.1:c.390C>T | ENSP00000508390.1:p.Pro130= | |
| ENST00000682577.1:c.390C>T | ENSP00000506963.1:p.Pro130= | |
| ENST00000682624.1:c.*34C>T | ENSP00000508343.1:n.*34C>T | |
| ENST00000682700.1:c.390C>T | ENSP00000507627.1:p.Pro130= | |
| ENST00000682804.1:n.283C>T | ||
| ENST00000682837.1:c.390C>T | ENSP00000507920.1:p.Pro130= | |
| ENST00000682935.1:n.390C>T | ||
| ENST00000682984.1:c.312+2694C>T | ENSP00000507209.1:n.312+2694C>T | |
| ENST00000683078.1:c.390C>T | ENSP00000506796.1:p.Pro130= | |
| ENST00000683223.1:c.301C>T | ENSP00000507685.1:n.301C>T | |
| ENST00000683238.1:n.211C>T | ||
| ENST00000683249.1:n.411C>T | ||
| ENST00000683336.1:c.390C>T | ENSP00000507695.1:p.Pro130= | |
| ENST00000683362.1:c.312+2694C>T | ENSP00000506985.1:n.312+2694C>T | |
| ENST00000683850.1:n.313C>T | ||
| ENST00000683919.1:c.390C>T | ENSP00000507617.1:p.Pro130= | |
| ENST00000683953.1:c.301C>T | ENSP00000508375.1:n.301C>T | |
| ENST00000684023.1:c.390C>T | ENSP00000507461.1:p.Pro130= | |
| ENST00000684064.1:c.81C>T | ENSP00000508192.1:p.Pro27= | |
| ENST00000684089.1:n.380C>T | ||
| ENST00000684149.1:c.390C>T | ENSP00000507943.1:p.Pro130= | |
| ENST00000684416.1:n.215C>T | ||
| ENST00000684540.1:c.390C>T | ENSP00000507987.1:p.Pro130= | |
| ENST00000684733.1:n.325C>T | ||
| ENST00000453321.8:c.390C>T MANE Select | ENSP00000389998.3:p.Pro130= | |
| ENST00000323130.7:c.360C>T | ENSP00000314488.3:p.Pro120= | |
| ENST00000409623.7:c.13C>T | ENSP00000386966.3:p.His5Tyr | |
| ENST00000452276.5:c.81C>T | ENSP00000388671.1:p.Pro27= | |
| ENST00000453321.7:c.390C>T | ENSP00000389998.3:p.Pro130= | |
| ENST00000453906.5:c.390C>T | ENSP00000403035.1:p.Pro130= | |
| ENST00000455946.5:c.390C>T | ENSP00000416339.1:p.Pro130= | |
| ENST00000474944.5:n.410C>T | ||
| ENST00000475305.1:n.399C>T | ||
| ENST00000498673.5:c.-91C>T | ENSP00000430232.1:n.-91C>T | |
| ENST00000518319.5:c.-130C>T | ENSP00000430289.1:n.-130C>T | |
| ENST00000521065.1:c.296C>T | ||
| ENST00000521222.5:c.*26C>T | ENSP00000429925.1:n.*26C>T | |
| ENST00000521517.5:c.382C>T | ||
| NM_001142301.1:c.13C>T , LRG_688t2:c.13C>T | NP_001135773.1:p.His5Tyr | |
| NM_153704.5:c.390C>T , LRG_688t1:c.390C>T | NP_714915.3:p.Pro130= | |
| NR_024522.1:n.461C>T | ||
| XM_006716686.2:c.87C>T | XP_006716749.1:p.Pro29= | |
| XM_011517363.1:c.390C>T | XP_011515665.1:p.Pro130= | |
| XR_428387.1:n.448C>T | ||
| XR_928360.1:n.448C>T | ||
| XR_928361.1:n.448C>T | ||
| XR_928362.1:n.448C>T | ||
| XM_006716686.4:c.87C>T | XP_006716749.1:p.Pro29= | |
| XM_011517363.3:c.390C>T | XP_011515665.1:p.Pro130= | |
| XM_024447326.1:c.-20C>T | XP_024303094.1:n.-20C>T | |
| XR_001745619.2:n.431C>T | ||
| XR_428387.2:n.431C>T | ||
| XR_928360.3:n.431C>T | ||
| XR_928362.3:n.431C>T | ||
| NM_153704.6:c.390C>T MANE Select | NP_714915.3:p.Pro130= | |
| NR_024522.2:n.411C>T |