Revel Score:
ENST00000394321
0.396
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7526579C>G , CM000681.2:g.7526579C>G | GRCh38 |
| NC_000019.9:g.7591465C>G , CM000681.1:g.7591465C>G | GRCh37 |
| NC_000019.8:g.7497465C>G | NCBI36 |
| NG_015806.1:g.8970C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.378C>G MANE Select | ENSP00000264079.5:p.Tyr126Ter | |
| ENST00000264079.10:c.378C>G | ENSP00000264079.5:p.Tyr126Ter | |
| ENST00000394321.9:n.458C>G | ||
| ENST00000596008.1:n.340C>G | ||
| ENST00000598406.1:n.199C>G | ||
| ENST00000601003.1:c.378C>G | ENSP00000469074.1:p.Tyr126Ter | |
| NM_020533.2:c.378C>G | NP_065394.1:p.Tyr126Ter | |
| NM_020533.3:c.378C>G MANE Select | NP_065394.1:p.Tyr126Ter |