Linked Data
ClinVar Variation Id:
1482519
ClinVar RCV Id:
RCV001995666
dbSNP Id:
rs934823566
gnomAD v4:
8-93758531-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93758531T>G , CM000670.2:g.93758531T>G | GRCh38 |
| NC_000008.10:g.94770759T>G , CM000670.1:g.94770759T>G | GRCh37 |
| NC_000008.9:g.94839935T>G | NCBI36 |
| NG_009190.1:g.8688T>G , LRG_688:g.8688T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.361T>G | ENSP00000314488.4:p.Leu121Val | |
| ENST00000409623.8:c.361T>G | ENSP00000386966.4:p.Leu121Val | |
| ENST00000452276.6:c.361T>G | ENSP00000388671.2:p.Leu121Val | |
| ENST00000453906.6:c.361T>G | ENSP00000403035.2:p.Leu121Val | |
| ENST00000520680.2:c.361T>G | ENSP00000428785.2:p.Leu121Val | |
| ENST00000521065.2:c.361T>G | ENSP00000427947.2:p.Leu121Val | |
| ENST00000521517.6:c.361T>G | ENSP00000430740.2:p.Leu121Val | |
| ENST00000681998.1:c.361T>G | ENSP00000506773.1:p.Leu121Val | |
| ENST00000682036.1:c.361T>G | ENSP00000508390.1:p.Leu121Val | |
| ENST00000682577.1:c.361T>G | ENSP00000506963.1:p.Leu121Val | |
| ENST00000682624.1:c.*5T>G | ENSP00000508343.1:n.*5T>G | |
| ENST00000682700.1:c.361T>G | ENSP00000507627.1:p.Leu121Val | |
| ENST00000682804.1:n.254T>G | ||
| ENST00000682837.1:c.361T>G | ENSP00000507920.1:p.Leu121Val | |
| ENST00000682935.1:n.361T>G | ||
| ENST00000682984.1:c.312+2665T>G | ENSP00000507209.1:n.312+2665T>G | |
| ENST00000683078.1:c.361T>G | ENSP00000506796.1:p.Leu121Val | |
| ENST00000683223.1:c.272T>G | ENSP00000507685.1:n.272T>G | |
| ENST00000683238.1:n.182T>G | ||
| ENST00000683249.1:n.382T>G | ||
| ENST00000683336.1:c.361T>G | ENSP00000507695.1:p.Leu121Val | |
| ENST00000683362.1:c.312+2665T>G | ENSP00000506985.1:n.312+2665T>G | |
| ENST00000683850.1:n.284T>G | ||
| ENST00000683919.1:c.361T>G | ENSP00000507617.1:p.Leu121Val | |
| ENST00000683953.1:c.272T>G | ENSP00000508375.1:n.272T>G | |
| ENST00000684023.1:c.361T>G | ENSP00000507461.1:p.Leu121Val | |
| ENST00000684064.1:c.52T>G | ENSP00000508192.1:p.Leu18Val | |
| ENST00000684089.1:n.351T>G | ||
| ENST00000684149.1:c.361T>G | ENSP00000507943.1:p.Leu121Val | |
| ENST00000684416.1:n.186T>G | ||
| ENST00000684540.1:c.361T>G | ENSP00000507987.1:p.Leu121Val | |
| ENST00000684733.1:n.296T>G | ||
| ENST00000453321.8:c.361T>G MANE Select | ENSP00000389998.3:p.Leu121Val | |
| ENST00000323130.7:c.331T>G | ENSP00000314488.3:p.Leu111Val | |
| ENST00000409623.7:c.-17T>G | ENSP00000386966.3:n.-17T>G | |
| ENST00000452276.5:c.52T>G | ENSP00000388671.1:p.Leu18Val | |
| ENST00000453321.7:c.361T>G | ENSP00000389998.3:p.Leu121Val | |
| ENST00000453906.5:c.361T>G | ENSP00000403035.1:p.Leu121Val | |
| ENST00000455946.5:c.361T>G | ENSP00000416339.1:p.Leu121Val | |
| ENST00000474944.5:n.381T>G | ||
| ENST00000475305.1:n.370T>G | ||
| ENST00000498673.5:c.-120T>G | ENSP00000430232.1:n.-120T>G | |
| ENST00000518319.5:c.-159T>G | ENSP00000430289.1:n.-159T>G | |
| ENST00000521065.1:c.267T>G | ||
| ENST00000521222.5:c.357T>G | ENSP00000429925.1:p.Thr119= | |
| ENST00000521517.5:c.353T>G | ||
| NM_001142301.1:c.-17T>G , LRG_688t2:c.-17T>G | NP_001135773.1:n.-17T>G | |
| NM_153704.5:c.361T>G , LRG_688t1:c.361T>G | NP_714915.3:p.Leu121Val | |
| NR_024522.1:n.432T>G | ||
| XM_006716686.2:c.58T>G | XP_006716749.1:p.Leu20Val | |
| XM_011517363.1:c.361T>G | XP_011515665.1:p.Leu121Val | |
| XR_428387.1:n.419T>G | ||
| XR_928360.1:n.419T>G | ||
| XR_928361.1:n.419T>G | ||
| XR_928362.1:n.419T>G | ||
| XM_006716686.4:c.58T>G | XP_006716749.1:p.Leu20Val | |
| XM_011517363.3:c.361T>G | XP_011515665.1:p.Leu121Val | |
| XM_024447326.1:c.-49T>G | XP_024303094.1:n.-49T>G | |
| XR_001745619.2:n.402T>G | ||
| XR_428387.2:n.402T>G | ||
| XR_928360.3:n.402T>G | ||
| XR_928362.3:n.402T>G | ||
| NM_153704.6:c.361T>G MANE Select | NP_714915.3:p.Leu121Val | |
| NR_024522.2:n.382T>G |