Linked Data
dbSNP Id:
rs745377828
ExAC:
6:7585299 T / G
gnomAD v2:
6-7585299-T-G
COSMIC:
COSM3875512
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7585066T>G , CM000668.2:g.7585066T>G | GRCh38 |
| NC_000006.11:g.7585299T>G , CM000668.1:g.7585299T>G | GRCh37 |
| NC_000006.10:g.7530298T>G | NCBI36 |
| NG_008803.1:g.48430T>G , LRG_423:g.48430T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.6475T>G | ENSP00000518230.1:p.Leu2159Val | |
| ENST00000379802.8:c.7804T>G MANE Select | ENSP00000369129.3:p.Leu2602Val | |
| ENST00000379802.7:c.7804T>G | ENSP00000369129.3:p.Leu2602Val | |
| ENST00000418664.2:c.6007T>G | ENSP00000396591.2:p.Leu2003Val | |
| NM_001008844.1:c.6007T>G | NP_001008844.1:p.Leu2003Val | |
| NM_004415.2:c.7804T>G , LRG_423t1:c.7804T>G | NP_004406.2:p.Leu2602Val | |
| XM_011514323.1:c.6475T>G | XP_011512625.1:p.Leu2159Val | |
| NM_001008844.2:c.6007T>G | NP_001008844.1:p.Leu2003Val | |
| NM_001319034.1:c.6475T>G | NP_001305963.1:p.Leu2159Val | |
| NM_004415.3:c.7804T>G | NP_004406.2:p.Leu2602Val | |
| NM_004415.4:c.7804T>G MANE Select | NP_004406.2:p.Leu2602Val | |
| NM_001008844.3:c.6007T>G | NP_001008844.1:p.Leu2003Val | |
| NM_001319034.2:c.6475T>G | NP_001305963.1:p.Leu2159Val |