Linked Data
ClinVar Variation Id:
183670
dbSNP Id:
rs781140315
gnomAD v2:
19-50332240-C-T
gnomAD v3:
19-49828983-C-T
gnomAD v4:
19-49828983-C-T
PubMed:
PMID:25527630
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49828983C>T , CM000681.2:g.49828983C>T | GRCh38 |
| NC_000019.9:g.50332240C>T , CM000681.1:g.50332240C>T | GRCh37 |
| NC_000019.8:g.55024052C>T | NCBI36 |
| NG_017091.1:g.15705C>T , LRG_368:g.15705C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593767.3:c.418C>T | ENSP00000470692.3:p.Arg140Trp | |
| ENST00000312865.10:c.418C>T MANE Select | ENSP00000326767.5:p.Arg140Trp | |
| ENST00000538643.5:c.181-1528C>T | ENSP00000437496.1:n.181-1528C>T | |
| ENST00000595185.5:c.418C>T | ENSP00000470027.1:p.Arg140Trp | |
| ENST00000612791.4:c.418C>T | ENSP00000479851.1:p.Arg140Trp | |
| ENST00000612854.4:c.418C>T | ENSP00000482155.1:p.Arg140Trp | |
| ENST00000617849.4:c.158-1756C>T | ENSP00000484882.1:n.158-1756C>T | |
| ENST00000618715.4:c.158-1755C>T | ENSP00000480731.1:n.158-1755C>T | |
| ENST00000620467.4:c.418C>T | ENSP00000482659.1:p.Arg140Trp | |
| ENST00000622402.4:c.146-6844C>T | ENSP00000478074.1:n.146-6844C>T | |
| NM_030973.3:c.418C>T , LRG_368t1:c.418C>T | NP_112235.2:p.Arg140Trp | |
| XM_011527353.1:c.418C>T | XP_011525655.1:p.Arg140Trp | |
| NM_001378355.1:c.418C>T | NP_001365284.1:p.Arg140Trp | |
| NM_030973.4:c.418C>T MANE Select | NP_112235.2:p.Arg140Trp |