Linked Data
ClinVar Variation Id:
156514
ClinVar RCV Id:
RCV000144661
dbSNP Id:
rs587783061
COSMIC:
COSM1667051
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1207062T>G , CM000681.2:g.1207062T>G | GRCh38 |
| NC_000019.9:g.1207061T>G , CM000681.1:g.1207061T>G | GRCh37 |
| NC_000019.8:g.1158061T>G | NCBI36 |
| NG_007460.2:g.22656T>G , LRG_319:g.22656T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.149T>G | ENSP00000490268.2:p.Leu50Arg | |
| ENST00000585748.3:c.-82-11355T>G | ENSP00000477641.2:n.-82-11355T>G | |
| ENST00000585851.2:c.149T>G | ENSP00000467912.2:p.Leu50Arg | |
| ENST00000326873.12:c.149T>G MANE Select | ENSP00000324856.6:p.Leu50Arg | |
| ENST00000652231.1:c.149T>G | ENSP00000498804.1:p.Leu50Arg | |
| ENST00000326873.11:c.149T>G | ENSP00000324856.6:p.Leu50Arg | |
| ENST00000585748.2:c.-82-11355T>G | ENSP00000477641.1:n.-82-11355T>G | |
| ENST00000585851.1:c.149T>G | ENSP00000467912.1:p.Leu50Arg | |
| ENST00000586243.5:c.149T>G | ENSP00000467240.2:p.Leu50Arg | |
| ENST00000589152.5:n.239T>G | ||
| ENST00000593219.5:c.149T>G | ENSP00000466610.1:p.Leu50Arg | |
| NM_000455.4:c.149T>G , LRG_319t1:c.149T>G | NP_000446.1:p.Leu50Arg | |
| XM_005259617.1:c.149T>G | XP_005259674.1:p.Leu50Arg | |
| XM_005259618.3:c.149T>G | XP_005259675.1:p.Leu50Arg | |
| XM_011528209.1:c.-205T>G | XP_011526511.1:n.-205T>G | |
| XR_936204.1:n.774T>G | ||
| XM_005259617.3:c.149T>G | XP_005259674.1:p.Leu50Arg | |
| XM_011528209.2:c.-205T>G | XP_011526511.1:n.-205T>G | |
| XR_001753738.2:n.774T>G | ||
| XR_001753739.1:n.774T>G | ||
| XR_001753740.2:n.774T>G | ||
| NM_000455.5:c.149T>G MANE Select | NP_000446.1:p.Leu50Arg |