Revel Score:
ENST00000362057 (MANE Select)
0.034
ENST00000374057
0.034
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00349664 (AFR)
Genomes Max Group AF
0.00349604 (AFR)
Exomes Max Group AF
0.00310747 (AFR)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.114504783C>G , CM000671.2:g.114504783C>G | GRCh38 |
| NC_000009.11:g.117267063C>G , CM000671.1:g.117267063C>G | GRCh37 |
| NC_000009.10:g.116306884C>G | NCBI36 |
| NG_016700.1:g.5674G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362057.4:c.19G>C MANE Select | ENSP00000354623.3:p.Gly7Arg | |
| ENST00000673697.1:c.19G>C | ENSP00000501152.1:p.Gly7Arg | |
| ENST00000362057.3:c.19G>C | ENSP00000354623.3:p.Gly7Arg | |
| ENST00000374057.3:c.19G>C | ENSP00000363170.3:p.Gly7Arg | |
| NM_001173425.1:c.19G>C | NP_001166896.1:p.Gly7Arg | |
| NM_015404.3:c.19G>C | NP_056219.3:p.Gly7Arg | |
| XM_005251897.3:c.19G>C | XP_005251954.2:p.Gly7Arg | |
| XM_011518484.1:c.19G>C | XP_011516786.1:p.Gly7Arg | |
| XM_011518485.1:c.19G>C | XP_011516787.1:p.Gly7Arg | |
| XM_011518486.1:c.19G>C | XP_011516788.1:p.Gly7Arg | |
| XM_011518487.1:c.19G>C | XP_011516789.1:p.Gly7Arg | |
| XM_011518488.1:c.19G>C | XP_011516790.1:p.Gly7Arg | |
| XM_011518489.1:c.19G>C | XP_011516791.1:p.Gly7Arg | |
| XM_011518490.1:c.19G>C | XP_011516792.1:p.Gly7Arg | |
| XM_011518491.1:c.19G>C | XP_011516793.1:p.Gly7Arg | |
| XM_011518492.1:c.19G>C | XP_011516794.1:p.Gly7Arg | |
| XM_011518493.1:c.19G>C | XP_011516795.1:p.Gly7Arg | |
| XM_011518494.1:c.19G>C | XP_011516796.1:p.Gly7Arg | |
| XR_929747.1:n.727G>C | ||
| XR_929748.1:n.727G>C | ||
| XR_929749.1:n.727G>C | ||
| XR_929750.1:n.727G>C | ||
| XR_929751.1:n.727G>C | ||
| XR_929752.1:n.727G>C | ||
| XR_929753.1:n.727G>C | ||
| XR_929754.1:n.727G>C | ||
| XR_929755.1:n.727G>C | ||
| XR_929756.1:n.727G>C | ||
| XR_929757.1:n.727G>C | ||
| XM_011518486.2:c.19G>C | XP_011516788.1:p.Gly7Arg | |
| XM_011518487.2:c.19G>C | XP_011516789.1:p.Gly7Arg | |
| XM_011518488.2:c.19G>C | XP_011516790.1:p.Gly7Arg | |
| XM_011518489.3:c.19G>C | XP_011516791.1:p.Gly7Arg | |
| XM_011518491.3:c.19G>C | XP_011516793.1:p.Gly7Arg | |
| XM_011518492.2:c.19G>C | XP_011516794.1:p.Gly7Arg | |
| XM_011518494.3:c.19G>C | XP_011516796.1:p.Gly7Arg | |
| XR_929747.2:n.38G>C | ||
| XR_929748.2:n.38G>C | ||
| XR_929749.2:n.38G>C | ||
| XR_929750.3:n.38G>C | ||
| XR_929752.2:n.38G>C | ||
| XR_929753.3:n.38G>C | ||
| XR_929754.2:n.38G>C | ||
| XR_929755.3:n.38G>C | ||
| XR_929756.2:n.38G>C | ||
| XR_929757.2:n.38G>C | ||
| NM_015404.4:c.19G>C MANE Select | NP_056219.3:p.Gly7Arg | |
| NM_001173425.2:c.19G>C | NP_001166896.1:p.Gly7Arg |