Revel Score:
ENST00000318351 (MANE Select)
0.330
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184060222G>T , CM000665.2:g.184060222G>T | GRCh38 |
| NC_000003.11:g.183778010G>T , CM000665.1:g.183778010G>T | GRCh37 |
| NC_000003.10:g.185260704G>T | NCBI36 |
| NG_012749.1:g.12176G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318351.2:c.1214G>T MANE Select | ENSP00000322617.1:p.Gly405Val | |
| ENST00000318351.1:c.1214G>T | ENSP00000322617.1:p.Gly405Val | |
| NM_130770.2:c.1214G>T | NP_570126.2:p.Gly405Val | |
| NM_130770.3:c.1214G>T MANE Select | NP_570126.2:p.Gly405Val |