Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12800471T>A , CM000681.2:g.12800471T>A | GRCh38 |
| NC_000019.9:g.12911285T>A , CM000681.1:g.12911285T>A | GRCh37 |
| NC_000019.8:g.12772285T>A | NCBI36 |
| NG_029901.1:g.6410A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005809.6:c.258-172A>T (PRDX2) MANE Select | NP_005800.3:n.258-172A>T |
| ENST00000301522.3:c.258-172A>T (PRDX2) MANE Select | ENSP00000301522.2:n.258-172A>T |
| NM_005809.5:c.258-172A>T (PRDX2) | NP_005800.3:n.258-172A>T |
| ENST00000301522.2:c.258-172A>T (PRDX2) | ENSP00000301522.2:n.258-172A>T |
| ENST00000334482.9:c.258-172A>T (PRDX2) | ENSP00000334063.5:n.258-172A>T |
| ENST00000466174.5:n.761A>T (PRDX2) | |
| ENST00000477555.1:n.316-172A>T (PRDX2) | |
| ENST00000589765.1:n.41+24707A>T (HOOK2) |