Revel Score:
ENST00000320868 (MANE Select)
0.630
gnomAD v2:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176754C>T , CM000678.2:g.176754C>T | GRCh38 |
| NC_000016.9:g.226753C>T , CM000678.1:g.226753C>T | GRCh37 |
| NC_000016.8:g.166753C>T | NCBI36 |
| NG_000006.1:g.37617C>T | |
| NG_059186.1:g.5104C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.38C>T MANE Select | ENSP00000322421.5:p.Ala13Val | |
| ENST00000397797.1:c.-10C>T | ENSP00000380899.1:n.-10C>T | |
| ENST00000472694.1:n.57C>T | ||
| ENST00000487791.1:n.7C>T | ||
| NM_000558.4:c.38C>T | NP_000549.1:p.Ala13Val | |
| NM_000558.5:c.38C>T MANE Select | NP_000549.1:p.Ala13Val |