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