Revel Score:
ENST00000204961 (MANE Select)
0.584
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68838684C>G , CM000685.2:g.68838684C>G | GRCh38 |
| NC_000023.10:g.68058527C>G , CM000685.1:g.68058527C>G | GRCh37 |
| NC_000023.9:g.67975252C>G | NCBI36 |
| NG_008887.1:g.14688C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.196C>G MANE Select | ENSP00000204961.4:p.Arg66Gly | |
| ENST00000204961.4:c.196C>G | ENSP00000204961.4:p.Arg66Gly | |
| NM_004429.4:c.196C>G | NP_004420.1:p.Arg66Gly | |
| NM_004429.5:c.196C>G MANE Select | NP_004420.1:p.Arg66Gly |