Linked Data
ClinVar Variation Id:
210986
dbSNP Id:
rs145762491
ExAC:
15:89838176 T / G
gnomAD v2:
15-89838176-T-G
gnomAD v3:
15-89294945-T-G
gnomAD v4:
15-89294945-T-G
COSMIC:
COSM3817013
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89294945T>G , CM000677.2:g.89294945T>G | GRCh38 |
| NC_000015.9:g.89838176T>G , CM000677.1:g.89838176T>G | GRCh37 |
| NC_000015.8:g.87639180T>G | NCBI36 |
| NG_011736.1:g.55983T>G , LRG_500:g.55983T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696717.1:c.2208T>G | ENSP00000512830.1:p.Leu736= | |
| ENST00000696718.1:c.1950T>G | ENSP00000512831.1:p.Leu650= | |
| ENST00000696719.1:c.2487T>G | ENSP00000512832.1:p.Leu829= | |
| ENST00000310775.12:c.2487T>G MANE Select | ENSP00000310842.8:p.Leu829= | |
| ENST00000674831.1:c.2487T>G | ENSP00000502474.1:p.Leu829= | |
| ENST00000676003.1:c.2457-12T>G | ENSP00000502254.1:n.2457-12T>G | |
| ENST00000300027.12:c.2456+948T>G | ENSP00000300027.8:n.2456+948T>G | |
| ENST00000310775.11:c.2487T>G | ENSP00000310842.7:p.Leu829= | |
| ENST00000447611.6:c.2456+948T>G | ENSP00000413249.2:n.2456+948T>G | |
| ENST00000561894.1:c.1935+948T>G | ||
| ENST00000565522.5:n.130-17959T>G | ||
| ENST00000566895.5:n.2494T>G | ||
| NM_001113378.1:c.2487T>G , LRG_500t1:c.2487T>G | NP_001106849.1:p.Leu829= | |
| NM_018193.2:c.2456+948T>G | NP_060663.2:n.2456+948T>G | |
| XM_011521756.1:c.2487T>G | XP_011520058.1:p.Leu829= | |
| XM_011521757.1:c.2487T>G | XP_011520059.1:p.Leu829= | |
| XM_011521758.1:c.2487T>G | XP_011520060.1:p.Leu829= | |
| XM_011521759.1:c.2487T>G | XP_011520061.1:p.Leu829= | |
| XM_011521760.1:c.2487T>G | XP_011520062.1:p.Leu829= | |
| XM_011521761.1:c.2487T>G | XP_011520063.1:p.Leu829= | |
| XM_011521762.1:c.2487T>G | XP_011520064.1:p.Leu829= | |
| XM_011521763.1:c.2457-12T>G | XP_011520065.1:n.2457-12T>G | |
| XM_011521764.1:c.2456+948T>G | XP_011520066.1:n.2456+948T>G | |
| XM_011521765.1:c.2208T>G | XP_011520067.1:p.Leu736= | |
| XM_011521766.1:c.2208T>G | XP_011520068.1:p.Leu736= | |
| XM_011521767.1:c.2208T>G | XP_011520069.1:p.Leu736= | |
| XM_011521768.1:c.2487T>G | XP_011520070.1:p.Leu829= | |
| XM_011521769.1:c.2291+1882T>G | XP_011520071.1:n.2291+1882T>G | |
| XM_011521756.2:c.2487T>G | XP_011520058.1:p.Leu829= | |
| XM_011521757.2:c.2487T>G | XP_011520059.1:p.Leu829= | |
| XM_011521764.2:c.2456+948T>G | XP_011520066.1:n.2456+948T>G | |
| XM_011521767.2:c.2208T>G | XP_011520069.1:p.Leu736= | |
| NM_001113378.2:c.2487T>G MANE Select | NP_001106849.1:p.Leu829= | |
| NM_001376910.1:c.2208T>G | NP_001363839.1:p.Leu736= | |
| NM_001376911.1:c.2487T>G | NP_001363840.1:p.Leu829= | |
| NM_018193.3:c.2456+948T>G | NP_060663.2:n.2456+948T>G |