Revel Score:
ENST00000356897 (MANE Select)
0.057
gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28503907A>T , CM000678.2:g.28503907A>T | GRCh38 |
| NC_000016.9:g.28515228A>T , CM000678.1:g.28515228A>T | GRCh37 |
| NC_000016.8:g.28422729A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356897.1:c.175T>A MANE Select | ENSP00000349365.1:p.Ser59Thr | |
| ENST00000568075.1:c.-219T>A | ENSP00000455990.1:n.-219T>A | |
| NM_145659.3:c.175T>A MANE Select | NP_663634.2:p.Ser59Thr | |
| XM_011545780.1:c.181T>A | XP_011544082.1:p.Ser61Thr | |
| XM_011545780.2:c.181T>A | XP_011544082.1:p.Ser61Thr |