gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.2339863 (AFR)
Genomes Max Group AF
0.2339863 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.44787134A>G , CM000684.2:g.44787134A>G | GRCh38 |
| NC_000022.10:g.45183014A>G , CM000684.1:g.45183014A>G | GRCh37 |
| NC_000022.9:g.43561678A>G | NCBI36 |
| NG_046967.1:g.89937A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356099.11:c.79+528A>G (ARHGAP8) MANE Select | ENSP00000348407.6:n.79+528A>G | |
| ENST00000336963.8:c.79+528A>G (ARHGAP8) | ENSP00000337287.4:n.79+528A>G | |
| ENST00000352766.11:c.841+528A>G (PRR5-ARHGAP8) | ENSP00000262731.11:n.841+528A>G | |
| ENST00000356099.10:c.79+528A>G (ARHGAP8) | ENSP00000348407.6:n.79+528A>G | |
| ENST00000361473.9:c.472+528A>G (PRR5-ARHGAP8) | ENSP00000354732.5:n.472+528A>G | |
| ENST00000389772.8:c.79+528A>G (ARHGAP8) | ENSP00000374422.4:n.79+528A>G | |
| ENST00000389774.6:c.79+528A>G (ARHGAP8) | ENSP00000374424.2:n.79+528A>G | |
| ENST00000396119.6:c.79+528A>G (ARHGAP8) | ENSP00000379425.2:n.79+528A>G | |
| ENST00000412433.5:c.79+528A>G (ARHGAP8) | ENSP00000402775.1:n.79+528A>G | |
| ENST00000447333.5:c.79+528A>G (ARHGAP8) | ENSP00000403618.1:n.79+528A>G | |
| ENST00000460809.5:n.204+528A>G (ARHGAP8) | ||
| ENST00000495219.1:n.55+528A>G (ARHGAP8) | ||
| ENST00000495250.2:n.255+528A>G (PRR5-ARHGAP8) | ||
| ENST00000515632.2:c.240+528A>G (PRR5-ARHGAP8) | ||
| NM_001017526.1:c.79+528A>G (ARHGAP8) | NP_001017526.1:n.79+528A>G | |
| NM_001198726.1:c.79+528A>G (ARHGAP8) | NP_001185655.1:n.79+528A>G | |
| NM_181334.5:c.472+528A>G (PRR5-ARHGAP8) | NP_851851.3:n.472+528A>G | |
| NM_181335.2:c.79+528A>G (ARHGAP8) | NP_851852.2:n.79+528A>G | |
| NM_001017526.2:c.79+528A>G (ARHGAP8) | NP_001017526.1:n.79+528A>G | |
| NM_001198726.2:c.79+528A>G (ARHGAP8) | NP_001185655.1:n.79+528A>G | |
| NM_181334.6:c.472+528A>G (PRR5-ARHGAP8) | NP_851851.3:n.472+528A>G | |
| NM_181335.3:c.79+528A>G (ARHGAP8) MANE Select | NP_851852.2:n.79+528A>G |