Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40161252T>G , CM000677.2:g.40161252T>G | GRCh38 |
| NC_000015.9:g.40453453T>G , CM000677.1:g.40453453T>G | GRCh37 |
| NC_000015.8:g.38240745T>G | NCBI36 |
| NG_016338.1:g.5244T>G , LRG_489:g.5244T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287598.11:c.32T>G MANE Select | ENSP00000287598.7:p.Leu11Arg | |
| ENST00000287598.10:c.32T>G | ENSP00000287598.6:p.Leu11Arg | |
| ENST00000412359.7:c.32T>G | ENSP00000398470.3:p.Leu11Arg | |
| ENST00000558715.5:c.32T>G | ENSP00000453861.1:p.Leu11Arg | |
| ENST00000559414.5:n.210T>G | ||
| ENST00000560120.5:n.230T>G | ||
| NM_001211.5:c.32T>G , LRG_489t1:c.32T>G | NP_001202.4:p.Leu11Arg | |
| NM_001211.6:c.32T>G MANE Select | NP_001202.5:p.Leu11Arg |