HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6996850G>A , CM000679.2:g.6996850G>A | GRCh38 |
NC_000017.10:g.6900169G>A , CM000679.1:g.6900169G>A | GRCh37 |
NC_000017.9:g.6840893G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.160G>A (ALOX12) MANE Select | ENSP00000251535.6:p.Ala54Thr | |
ENST00000251535.10:c.160G>A (ALOX12) | ENSP00000251535.6:p.Ala54Thr | |
NM_000697.2:c.160G>A (ALOX12) | NP_000688.2:p.Ala54Thr | |
NR_040089.1:n.234-11310C>T (ALOX12-AS1) | ||
XM_011523780.1:c.517G>A (ALOX12) | XP_011522082.1:p.Ala173Thr | |
XM_011523780.2:c.517G>A (ALOX12) | XP_011522082.1:p.Ala173Thr | |
NM_000697.3:c.160G>A (ALOX12) MANE Select | NP_000688.2:p.Ala54Thr |