Revel Score:
ENST00000308868 (MANE Select)
0.146
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128254539G>C , CM000669.2:g.128254539G>C | GRCh38 |
| NC_000007.13:g.127894592G>C , CM000669.1:g.127894592G>C | GRCh37 |
| NC_000007.12:g.127681828G>C | NCBI36 |
| NG_007450.1:g.18262G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308868.5:c.280G>C MANE Select | ENSP00000312652.4:p.Val94Leu | |
| ENST00000308868.4:c.280G>C | ENSP00000312652.4:p.Val94Leu | |
| NM_000230.2:c.280G>C | NP_000221.1:p.Val94Leu | |
| XM_005250340.3:c.277G>C | XP_005250397.1:p.Val93Leu | |
| XM_005250340.5:c.277G>C | XP_005250397.1:p.Val93Leu | |
| NM_000230.3:c.280G>C MANE Select | NP_000221.1:p.Val94Leu |