Linked Data
ClinVar Variation Id:
659
dbSNP Id:
rs121918143
ExAC:
2:128183756 C / T
gnomAD v2:
2-128183756-C-T
gnomAD v3:
2-127426180-C-T
gnomAD v4:
2-127426180-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.127426180C>T , CM000664.2:g.127426180C>T | GRCh38 |
| NC_000002.11:g.128183756C>T , CM000664.1:g.128183756C>T | GRCh37 |
| NC_000002.10:g.127900226C>T | NCBI36 |
| NG_016323.1:g.12761C>T , LRG_599:g.12761C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234071.8:c.631C>T MANE Select | ENSP00000234071.4:p.Arg211Trp | |
| ENST00000234071.7:c.631C>T | ENSP00000234071.3:p.Arg211Trp | |
| ENST00000402125.2:c.121-2177C>T | ||
| ENST00000409048.1:c.733C>T | ENSP00000386679.1:p.Arg245Trp | |
| ENST00000464089.1:n.217C>T | ||
| NM_000312.3:c.631C>T , LRG_599t1:c.631C>T | NP_000303.1:p.Arg211Trp | |
| XM_005263715.3:c.814C>T | XP_005263772.1:p.Arg272Trp | |
| XM_005263716.3:c.796C>T | XP_005263773.1:p.Arg266Trp | |
| XM_005263717.3:c.694C>T | XP_005263774.1:p.Arg232Trp | |
| XM_005263717.4:c.694C>T | XP_005263774.1:p.Arg232Trp | |
| XM_017004505.1:c.874C>T | XP_016859994.1:p.Arg292Trp | |
| XM_024453002.1:c.976C>T | XP_024308770.1:p.Arg326Trp | |
| XM_024453003.1:c.916C>T | XP_024308771.1:p.Arg306Trp | |
| XM_024453004.1:c.814C>T | XP_024308772.1:p.Arg272Trp | |
| XM_024453005.1:c.796C>T | XP_024308773.1:p.Arg266Trp | |
| XM_024453006.1:c.733C>T | XP_024308774.1:p.Arg245Trp | |
| XR_923313.2:n.4405G>A | ||
| NM_000312.4:c.631C>T MANE Select | NP_000303.1:p.Arg211Trp | |
| NM_001375602.1:c.814C>T | NP_001362531.1:p.Arg272Trp | |
| NM_001375603.1:c.796C>T | NP_001362532.1:p.Arg266Trp | |
| NM_001375604.1:c.694C>T | NP_001362533.1:p.Arg232Trp | |
| NM_001375605.1:c.733C>T | NP_001362534.1:p.Arg245Trp | |
| NM_001375606.1:c.799C>T | NP_001362535.1:p.Arg267Trp | |
| NM_001375607.1:c.817C>T | NP_001362536.1:p.Arg273Trp | |
| NM_001375608.1:c.574C>T | NP_001362537.1:p.Arg192Trp | |
| NM_001375609.1:c.607C>T | NP_001362538.1:p.Arg203Trp | |
| NM_001375610.1:c.625C>T | NP_001362539.1:p.Arg209Trp | |
| NM_001375611.1:c.631C>T | NP_001362540.1:p.Arg211Trp | |
| NM_001375613.1:c.631C>T | NP_001362542.1:p.Arg211Trp |