ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.07755077 (AFR)
Genomes Max Group AF
0.07773945 (AFR)
Exomes Max Group AF
0.07403045 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102231446G>C , CM000672.2:g.102231446G>C | GRCh38 |
| NC_000010.10:g.103991203G>C , CM000672.1:g.103991203G>C | GRCh37 |
| NC_000010.9:g.103981193G>C | NCBI36 |
| NG_008147.1:g.15029C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370002.8:c.321+142C>G (PITX3) MANE Select | ENSP00000359019.3:n.321+142C>G | |
| ENST00000370002.7:c.321+142C>G (PITX3) | ENSP00000359019.3:n.321+142C>G | |
| ENST00000539804.1:c.321+142C>G (PITX3) | ENSP00000439383.1:n.321+142C>G | |
| NM_005029.3:c.321+142C>G (PITX3) | NP_005020.1:n.321+142C>G | |
| XM_011539865.1:c.339+142C>G (PITX3) | XP_011538167.1:n.339+142C>G | |
| NM_005029.4:c.321+142C>G (PITX3) MANE Select | NP_005020.1:n.321+142C>G | |
| NM_001391923.1:c.-11+530G>C (GBF1) | NP_001378852.1:n.-11+530G>C | |
| NM_001391924.1:c.-149+530G>C (GBF1) | NP_001378853.1:n.-149+530G>C |