Revel Score:
ENST00000204961 (MANE Select)
0.955
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68839708G>A , CM000685.2:g.68839708G>A | GRCh38 |
| NC_000023.10:g.68059551G>A , CM000685.1:g.68059551G>A | GRCh37 |
| NC_000023.9:g.67976276G>A | NCBI36 |
| NG_008887.1:g.15712G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.451G>A MANE Select | ENSP00000204961.4:p.Gly151Ser | |
| ENST00000204961.4:c.451G>A | ENSP00000204961.4:p.Gly151Ser | |
| NM_004429.4:c.451G>A | NP_004420.1:p.Gly151Ser | |
| NM_004429.5:c.451G>A MANE Select | NP_004420.1:p.Gly151Ser |