Revel Score:
ENST00000307503 (MANE Select)
0.849
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869171T>G , CM000664.2:g.240869171T>G | GRCh38 |
| NC_000002.11:g.241808588T>G , CM000664.1:g.241808588T>G | GRCh37 |
| NC_000002.10:g.241457261T>G | NCBI36 |
| NG_008005.1:g.5427T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.167T>G MANE Select | ENSP00000302620.3:p.Ile56Ser | |
| ENST00000307503.3:c.167T>G | ENSP00000302620.3:p.Ile56Ser | |
| ENST00000472436.1:n.187T>G | ||
| NM_000030.2:c.167T>G | NP_000021.1:p.Ile56Ser | |
| XR_924060.1:n.405+1062A>C | ||
| NM_000030.3:c.167T>G MANE Select | NP_000021.1:p.Ile56Ser |