Linked Data
ClinVar Variation Id:
2187628
ClinVar RCV Id:
RCV002615906
dbSNP Id:
rs1206446041
gnomAD v2:
2-145156919-G-A
gnomAD v3:
2-144399352-G-A
gnomAD v4:
2-144399352-G-A
COSMIC:
COSM3425256
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.144399352G>A , CM000664.2:g.144399352G>A | GRCh38 |
| NC_000002.11:g.145156919G>A , CM000664.1:g.145156919G>A | GRCh37 |
| NC_000002.10:g.144873389G>A | NCBI36 |
| NG_016431.1:g.126040C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689298.1:c.*1684C>T | ENSP00000508434.1:n.*1684C>T | |
| ENST00000440875.6:c.1058C>T | ENSP00000475553.3:p.Ala353Val | |
| ENST00000627532.3:c.1835C>T MANE Select | ENSP00000487174.1:p.Ala612Val | |
| ENST00000636026.2:c.1835C>T | ENSP00000490776.1:p.Ala612Val | |
| ENST00000636179.1:n.1804C>T | ||
| ENST00000636413.1:c.1499C>T | ENSP00000490508.1:p.Ala500Val | |
| ENST00000636471.1:c.1910C>T | ENSP00000490317.1:p.Ala637Val | |
| ENST00000636732.2:c.*1552C>T | ENSP00000490175.1:n.*1552C>T | |
| ENST00000636820.1:n.1935C>T | ||
| ENST00000637045.1:c.1499C>T | ENSP00000490141.1:p.Ala500Val | |
| ENST00000637267.2:c.1835C>T | ENSP00000490293.2:p.Ala612Val | |
| ENST00000637304.1:c.1499C>T | ENSP00000490872.1:p.Ala500Val | |
| ENST00000638007.1:c.1499C>T | ENSP00000490723.1:p.Ala500Val | |
| ENST00000638087.1:c.1499C>T | ENSP00000490673.1:p.Ala500Val | |
| ENST00000638128.1:c.1058C>T | ENSP00000490934.1:p.Ala353Val | |
| ENST00000675069.1:c.-133-502C>T | ENSP00000502467.1:n.-133-502C>T | |
| ENST00000675145.1:n.2383C>T | ||
| ENST00000303660.8:c.1832C>T | ENSP00000302501.4:p.Ala611Val | |
| ENST00000409487.7:c.1835C>T | ENSP00000386854.2:p.Ala612Val | |
| ENST00000419938.5:c.655+1847C>T | ENSP00000394777.2:n.655+1847C>T | |
| ENST00000427902.5:c.1922C>T | ENSP00000395496.2:p.Ala641Val | |
| ENST00000440875.5:c.1167+185C>T | ENSP00000475553.2:n.1167+185C>T | |
| ENST00000539609.7:c.1763C>T | ENSP00000443792.2:p.Ala588Val | |
| ENST00000558170.6:c.1835C>T | ENSP00000454157.1:p.Ala612Val | |
| ENST00000627532.2:c.1835C>T | ENSP00000487174.1:p.Ala612Val | |
| NM_001171653.1:c.1763C>T | NP_001165124.1:p.Ala588Val | |
| NM_014795.3:c.1835C>T | NP_055610.1:p.Ala612Val | |
| XM_006712881.2:c.1835C>T | XP_006712944.1:p.Ala612Val | |
| XM_006712882.2:c.1835C>T | XP_006712945.1:p.Ala612Val | |
| XM_011512231.1:c.1826C>T | XP_011510533.1:p.Ala609Val | |
| XM_011512232.1:c.1814C>T | XP_011510534.1:p.Ala605Val | |
| NM_014795.4:c.1835C>T MANE Select | NP_055610.1:p.Ala612Val | |
| NM_001171653.2:c.1763C>T | NP_001165124.1:p.Ala588Val |