gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.29129222 (EAS)
Genomes Max Group AF
0.29129222 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94256104T>C , CM000663.2:g.94256104T>C | GRCh38 |
| NC_000001.10:g.94721660T>C , CM000663.1:g.94721660T>C | GRCh37 |
| NC_000001.9:g.94494248T>C | NCBI36 |
| NG_050965.1:g.23965A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000552844.5:c.-33+18908A>G (ARHGAP29) | ENSP00000449764.1:n.-33+18908A>G | |
| XM_011542439.1:c.-33+18908A>G (ARHGAP29) | XP_011540741.1:n.-33+18908A>G | |
| XM_011542439.2:c.-33+18908A>G (ARHGAP29) | XP_011540741.1:n.-33+18908A>G | |
| XR_001738151.2:n.328+6585T>C (ARHGAP29-AS1) | ||
| XR_001738152.2:n.449+5560T>C (ARHGAP29-AS1) | ||
| XR_001738153.2:n.545+5560T>C (ARHGAP29-AS1) | ||
| XR_001738154.1:n.502+5560T>C (ARHGAP29-AS1) | ||
| XR_001738157.1:n.289+6585T>C (ARHGAP29-AS1) | ||
| XR_002958338.1:n.375+6585T>C (ARHGAP29-AS1) |