Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6997021G= , CM000679.2:g.6997021G= | GRCh38 |
| NC_000017.10:g.6900340G= , CM000679.1:g.6900340G= | GRCh37 |
| NC_000017.9:g.6841064G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251535.11:c.331G= (ALOX12) MANE Select | ENSP00000251535.6:p.Gly111= | |
| ENST00000251535.10:c.331G= (ALOX12) | ENSP00000251535.6:p.Gly111= | |
| ENST00000480801.1:c.40G= (ALOX12) | ENSP00000467033.1:p.Gly14= | |
| NM_000697.2:c.331G= (ALOX12) | NP_000688.2:p.Gly111= | |
| NR_040089.1:n.234-11481C= (ALOX12-AS1) | ||
| XM_011523780.1:c.688G= (ALOX12) | XP_011522082.1:p.Gly230= | |
| XM_011523780.2:c.688G= (ALOX12) | XP_011522082.1:p.Gly230= | |
| NM_000697.3:c.331G= (ALOX12) MANE Select | NP_000688.2:p.Gly111= |