HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6997024A>G , CM000679.2:g.6997024A>G | GRCh38 |
NC_000017.10:g.6900343A>G , CM000679.1:g.6900343A>G | GRCh37 |
NC_000017.9:g.6841067A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.334A>G (ALOX12) MANE Select | ENSP00000251535.6:p.Thr112Ala | |
ENST00000251535.10:c.334A>G (ALOX12) | ENSP00000251535.6:p.Thr112Ala | |
ENST00000480801.1:c.43A>G (ALOX12) | ENSP00000467033.1:p.Thr15Ala | |
NM_000697.2:c.334A>G (ALOX12) | NP_000688.2:p.Thr112Ala | |
NR_040089.1:n.234-11484T>C (ALOX12-AS1) | ||
XM_011523780.1:c.691A>G (ALOX12) | XP_011522082.1:p.Thr231Ala | |
XM_011523780.2:c.691A>G (ALOX12) | XP_011522082.1:p.Thr231Ala | |
NM_000697.3:c.334A>G (ALOX12) MANE Select | NP_000688.2:p.Thr112Ala |