Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6996687T= , CM000679.2:g.6996687T= | GRCh38 |
| NC_000017.10:g.6900006T= , CM000679.1:g.6900006T= | GRCh37 |
| NC_000017.9:g.6840730T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251535.11:c.136-139T= (ALOX12) MANE Select | ENSP00000251535.6:n.136-139T= | |
| ENST00000251535.10:c.136-139T= (ALOX12) | ENSP00000251535.6:n.136-139T= | |
| NM_000697.2:c.136-139T= (ALOX12) | NP_000688.2:n.136-139T= | |
| NR_040089.1:n.234-11147A= (ALOX12-AS1) | ||
| XM_011523780.1:c.493-139T= (ALOX12) | XP_011522082.1:n.493-139T= | |
| XM_011523780.2:c.493-139T= (ALOX12) | XP_011522082.1:n.493-139T= | |
| NM_000697.3:c.136-139T= (ALOX12) MANE Select | NP_000688.2:n.136-139T= |