dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.47382468 (AFR)
Genomes Max Group AF
0.47011047 (AFR)
Exomes Max Group AF
0.47644666 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12800471T>C , CM000681.2:g.12800471T>C | GRCh38 |
| NC_000019.9:g.12911285T>C , CM000681.1:g.12911285T>C | GRCh37 |
| NC_000019.8:g.12772285T>C | NCBI36 |
| NG_029901.1:g.6410A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301522.3:c.258-172A>G (PRDX2) MANE Select | ENSP00000301522.2:n.258-172A>G | |
| ENST00000301522.2:c.258-172A>G (PRDX2) | ENSP00000301522.2:n.258-172A>G | |
| ENST00000334482.9:c.258-172A>G (PRDX2) | ENSP00000334063.5:n.258-172A>G | |
| ENST00000466174.5:n.761A>G (PRDX2) | ||
| ENST00000477555.1:n.316-172A>G (PRDX2) | ||
| ENST00000589765.1:n.41+24707A>G (HOOK2) | ||
| NM_005809.5:c.258-172A>G (PRDX2) | NP_005800.3:n.258-172A>G | |
| NM_005809.6:c.258-172A>G (PRDX2) MANE Select | NP_005800.3:n.258-172A>G |