Revel Score:
ENST00000378970 (MANE Select)
0.165
ENST00000453287
0.165
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30309255G>C , CM000685.2:g.30309255G>C | GRCh38 |
| NC_000023.10:g.30327372G>C , CM000685.1:g.30327372G>C | GRCh37 |
| NC_000023.9:g.30237293G>C | NCBI36 |
| NG_009814.1:g.5124C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.109C>G MANE Select | ENSP00000368253.4:p.Gln37Glu | |
| ENST00000378970.4:c.109C>G | ENSP00000368253.4:p.Gln37Glu | |
| NM_000475.4:c.109C>G | NP_000466.2:p.Gln37Glu | |
| NM_000475.5:c.109C>G MANE Select | NP_000466.2:p.Gln37Glu |