Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6997026C>G , CM000679.2:g.6997026C>G | GRCh38 |
| NC_000017.10:g.6900345C>G , CM000679.1:g.6900345C>G | GRCh37 |
| NC_000017.9:g.6841069C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251535.11:c.336C>G (ALOX12) MANE Select | ENSP00000251535.6:p.Thr112= | |
| ENST00000251535.10:c.336C>G (ALOX12) | ENSP00000251535.6:p.Thr112= | |
| ENST00000480801.1:c.45C>G (ALOX12) | ENSP00000467033.1:p.Thr15= | |
| NM_000697.2:c.336C>G (ALOX12) | NP_000688.2:p.Thr112= | |
| NR_040089.1:n.234-11486G>C (ALOX12-AS1) | ||
| XM_011523780.1:c.693C>G (ALOX12) | XP_011522082.1:p.Thr231= | |
| XM_011523780.2:c.693C>G (ALOX12) | XP_011522082.1:p.Thr231= | |
| NM_000697.3:c.336C>G (ALOX12) MANE Select | NP_000688.2:p.Thr112= |