gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.47098616 (AFR)
Genomes Max Group AF
0.47098616 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12801582A>C , CM000681.2:g.12801582A>C | GRCh38 |
| NC_000019.9:g.12912396A>C , CM000681.1:g.12912396A>C | GRCh37 |
| NC_000019.8:g.12773396A>C | NCBI36 |
| NG_029901.1:g.5299T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301522.3:c.-10+158T>G (PRDX2) MANE Select | ENSP00000301522.2:n.-10+158T>G | |
| ENST00000301522.2:c.-10+158T>G (PRDX2) | ENSP00000301522.2:n.-10+158T>G | |
| ENST00000334482.9:c.-10+158T>G (PRDX2) | ENSP00000334063.5:n.-10+158T>G | |
| ENST00000466174.5:n.50+158T>G (PRDX2) | ||
| ENST00000477555.1:n.49+158T>G (PRDX2) | ||
| ENST00000589765.1:n.41+23596T>G (HOOK2) | ||
| NM_005809.5:c.-10+158T>G (PRDX2) | NP_005800.3:n.-10+158T>G | |
| NM_005809.6:c.-10+158T>G (PRDX2) MANE Select | NP_005800.3:n.-10+158T>G |