Linked Data
ClinVar Variation Id:
2991195
ClinVar RCV Id:
RCV003849858
dbSNP Id:
rs730881179
gnomAD v4:
2-144398692-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.144398692G>A , CM000664.2:g.144398692G>A | GRCh38 |
| NC_000002.11:g.145156259G>A , CM000664.1:g.145156259G>A | GRCh37 |
| NC_000002.10:g.144872729G>A | NCBI36 |
| NG_016431.1:g.126700C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000689298.1:c.*2344C>T | ENSP00000508434.1:n.*2344C>T | |
| ENST00000440875.6:c.1718C>T | ENSP00000475553.3:p.Ala573Val | |
| ENST00000627532.3:c.2495C>T MANE Select | ENSP00000487174.1:p.Ala832Val | |
| ENST00000636026.2:c.2495C>T | ENSP00000490776.1:p.Ala832Val | |
| ENST00000636179.1:n.2464C>T | ||
| ENST00000636413.1:c.2159C>T | ENSP00000490508.1:p.Ala720Val | |
| ENST00000636471.1:c.2570C>T | ENSP00000490317.1:p.Ala857Val | |
| ENST00000636732.2:c.*2212C>T | ENSP00000490175.1:n.*2212C>T | |
| ENST00000636820.1:n.2595C>T | ||
| ENST00000637045.1:c.2159C>T | ENSP00000490141.1:p.Ala720Val | |
| ENST00000637304.1:c.2159C>T | ENSP00000490872.1:p.Ala720Val | |
| ENST00000638007.1:c.2159C>T | ENSP00000490723.1:p.Ala720Val | |
| ENST00000638087.1:c.2159C>T | ENSP00000490673.1:p.Ala720Val | |
| ENST00000638128.1:c.1718C>T | ENSP00000490934.1:p.Ala573Val | |
| ENST00000675069.1:c.26C>T | ENSP00000502467.1:p.Ala9Val | |
| ENST00000303660.8:c.2492C>T | ENSP00000302501.4:p.Ala831Val | |
| ENST00000409487.7:c.2495C>T | ENSP00000386854.2:p.Ala832Val | |
| ENST00000419938.5:c.655+2507C>T | ENSP00000394777.2:n.655+2507C>T | |
| ENST00000440875.5:c.1168-764C>T | ENSP00000475553.2:n.1168-764C>T | |
| ENST00000539609.7:c.2423C>T | ENSP00000443792.2:p.Ala808Val | |
| ENST00000558170.6:c.2495C>T | ENSP00000454157.1:p.Ala832Val | |
| ENST00000627532.2:c.2495C>T | ENSP00000487174.1:p.Ala832Val | |
| NM_001171653.1:c.2423C>T | NP_001165124.1:p.Ala808Val | |
| NM_014795.3:c.2495C>T | NP_055610.1:p.Ala832Val | |
| XM_006712881.2:c.2495C>T | XP_006712944.1:p.Ala832Val | |
| XM_006712882.2:c.2495C>T | XP_006712945.1:p.Ala832Val | |
| XM_011512231.1:c.2486C>T | XP_011510533.1:p.Ala829Val | |
| XM_011512232.1:c.2474C>T | XP_011510534.1:p.Ala825Val | |
| NM_014795.4:c.2495C>T MANE Select | NP_055610.1:p.Ala832Val | |
| NM_001171653.2:c.2423C>T | NP_001165124.1:p.Ala808Val |