Revel Score:
ENST00000255040 (MANE Select)
0.119
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.159588367G>T , CM000663.2:g.159588367G>T | GRCh38 |
| NC_000001.10:g.159558157G>T , CM000663.1:g.159558157G>T | GRCh37 |
| NC_000001.9:g.157824781G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255040.3:c.331G>T MANE Select | ENSP00000255040.2:p.Val111Leu | |
| ENST00000255040.2:c.331G>T | ENSP00000255040.2:p.Val111Leu | |
| NM_001639.3:c.331G>T | NP_001630.1:p.Val111Leu | |
| NM_001639.4:c.331G>T MANE Select | NP_001630.1:p.Val111Leu |