Revel Score:
ENST00000320868 (MANE Select)
0.535
ENST00000397797
0.535
gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177319C>G , CM000678.2:g.177319C>G | GRCh38 |
| NC_000016.9:g.227318C>G , CM000678.1:g.227318C>G | GRCh37 |
| NC_000016.8:g.167318C>G | NCBI36 |
| NG_000006.1:g.38182C>G | |
| NG_059186.1:g.5669C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.337C>G MANE Select | ENSP00000322421.5:p.His113Asp | |
| ENST00000397797.1:c.241C>G | ENSP00000380899.1:p.His81Asp | |
| ENST00000472694.1:n.473C>G | ||
| NM_000558.4:c.337C>G | NP_000549.1:p.His113Asp | |
| NM_000558.5:c.337C>G MANE Select | NP_000549.1:p.His113Asp |