Linked Data
ClinVar Variation Id:
217717
dbSNP Id:
rs751517725
gnomAD v2:
8-94815880-C-T
gnomAD v3:
8-93803652-C-T
gnomAD v4:
8-93803652-C-T
PubMed:
PMID:26092869
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93803652C>T , CM000670.2:g.93803652C>T | GRCh38 |
| NC_000008.10:g.94815880C>T , CM000670.1:g.94815880C>T | GRCh37 |
| NC_000008.9:g.94885056C>T | NCBI36 |
| NG_009190.1:g.53809C>T , LRG_688:g.53809C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.2290C>T | ENSP00000314488.4:p.Arg764Ter | |
| ENST00000409623.8:c.2245C>T | ENSP00000386966.4:p.Arg749Ter | |
| ENST00000452276.6:c.2290C>T | ENSP00000388671.2:p.Arg764Ter | |
| ENST00000453906.6:c.1408C>T | ENSP00000403035.2:p.Arg470Ter | |
| ENST00000518896.2:c.581C>T | ENSP00000507992.1:n.581C>T | |
| ENST00000520680.2:c.2413C>T | ENSP00000428785.2:p.Arg805Ter | |
| ENST00000521517.6:c.2191C>T | ENSP00000430740.2:p.Arg731Ter | |
| ENST00000681998.1:c.2111C>T | ENSP00000506773.1:n.2111C>T | |
| ENST00000682036.1:c.1531C>T | ENSP00000508390.1:p.Arg511Ter | |
| ENST00000682577.1:c.2063C>T | ENSP00000506963.1:n.2063C>T | |
| ENST00000682624.1:c.*1864C>T | ENSP00000508343.1:n.*1864C>T | |
| ENST00000682700.1:c.2290C>T | ENSP00000507627.1:p.Arg764Ter | |
| ENST00000682744.1:n.1828C>T | ||
| ENST00000682804.1:n.2113C>T | ||
| ENST00000682837.1:c.1779C>T | ENSP00000507920.1:n.1779C>T | |
| ENST00000682935.1:n.4340C>T | ||
| ENST00000682984.1:c.1951C>T | ENSP00000507209.1:p.Arg651Ter | |
| ENST00000683078.1:c.2045C>T | ENSP00000506796.1:n.2045C>T | |
| ENST00000683223.1:c.2022C>T | ENSP00000507685.1:n.2022C>T | |
| ENST00000683238.1:n.3514C>T | ||
| ENST00000683249.1:n.3887C>T | ||
| ENST00000683336.1:c.2111C>T | ENSP00000507695.1:n.2111C>T | |
| ENST00000683362.1:c.1951C>T | ENSP00000506985.1:p.Arg651Ter | |
| ENST00000683850.1:n.2213C>T | ||
| ENST00000683919.1:c.2220C>T | ENSP00000507617.1:n.2220C>T | |
| ENST00000683953.1:c.2201C>T | ENSP00000508375.1:n.2201C>T | |
| ENST00000684023.1:c.2267C>T | ENSP00000507461.1:n.2267C>T | |
| ENST00000684064.1:c.1981C>T | ENSP00000508192.1:p.Arg661Ter | |
| ENST00000684089.1:n.3840C>T | ||
| ENST00000684149.1:c.*1469C>T | ENSP00000507943.1:n.*1469C>T | |
| ENST00000684343.1:c.487C>T | ENSP00000507591.1:p.Arg163Ter | |
| ENST00000684416.1:n.2249C>T | ||
| ENST00000684540.1:c.2220C>T | ENSP00000507987.1:n.2220C>T | |
| ENST00000453321.8:c.2290C>T MANE Select | ENSP00000389998.3:p.Arg764Ter | |
| ENST00000323130.7:c.2260C>T | ENSP00000314488.3:p.Arg754Ter | |
| ENST00000409623.7:c.2047C>T | ENSP00000386966.3:p.Arg683Ter | |
| ENST00000453321.7:c.2290C>T | ENSP00000389998.3:p.Arg764Ter | |
| ENST00000474944.5:n.1428C>T | ||
| ENST00000519845.5:n.1022C>T | ||
| NM_001142301.1:c.2047C>T , LRG_688t2:c.2047C>T | NP_001135773.1:p.Arg683Ter | |
| NM_153704.5:c.2290C>T , LRG_688t1:c.2290C>T | NP_714915.3:p.Arg764Ter | |
| NR_024522.1:n.2361C>T | ||
| XM_006716686.2:c.1987C>T | XP_006716749.1:p.Arg663Ter | |
| XM_006716687.2:c.1690C>T | XP_006716750.1:p.Arg564Ter | |
| XM_011517363.1:c.1408C>T | XP_011515665.1:p.Arg470Ter | |
| XR_428387.1:n.2348C>T | ||
| XR_928360.1:n.2348C>T | ||
| XR_928361.1:n.2348C>T | ||
| XR_928362.1:n.2348C>T | ||
| XM_006716686.4:c.1987C>T | XP_006716749.1:p.Arg663Ter | |
| XM_011517363.3:c.1408C>T | XP_011515665.1:p.Arg470Ter | |
| XM_024447326.1:c.1636C>T | XP_024303094.1:p.Arg546Ter | |
| XR_001745619.2:n.2331C>T | ||
| XR_428387.2:n.2331C>T | ||
| XR_928360.3:n.2331C>T | ||
| XR_928362.3:n.2331C>T | ||
| NM_153704.6:c.2290C>T MANE Select | NP_714915.3:p.Arg764Ter | |
| NR_024522.2:n.2311C>T |