Revel Score:
ENST00000176183 (MANE Select)
0.112
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.640119C>G , CM000673.2:g.640119C>G | GRCh38 |
| NC_000011.9:g.640119C>G , CM000673.1:g.640119C>G | GRCh37 |
| NC_000011.8:g.630119C>G | NCBI36 |
| NG_021241.1:g.7815C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000176183.6:c.870C>G MANE Select | ENSP00000176183.5:p.Cys290Trp | |
| ENST00000176183.5:c.870C>G | ENSP00000176183.5:p.Cys290Trp | |
| NM_000797.3:c.870C>G | NP_000788.2:p.Cys290Trp | |
| NM_000797.4:c.870C>G MANE Select | NP_000788.2:p.Cys290Trp |