HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6996984C>G , CM000679.2:g.6996984C>G | GRCh38 |
NC_000017.10:g.6900303C>G , CM000679.1:g.6900303C>G | GRCh37 |
NC_000017.9:g.6841027C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.294C>G (ALOX12) MANE Select | ENSP00000251535.6:p.Arg98= | |
ENST00000251535.10:c.294C>G (ALOX12) | ENSP00000251535.6:p.Arg98= | |
ENST00000480801.1:c.3C>G (ALOX12) | ENSP00000467033.1:p.Arg1= | |
NM_000697.2:c.294C>G (ALOX12) | NP_000688.2:p.Arg98= | |
NR_040089.1:n.234-11444G>C (ALOX12-AS1) | ||
XM_011523780.1:c.651C>G (ALOX12) | XP_011522082.1:p.Arg217= | |
XM_011523780.2:c.651C>G (ALOX12) | XP_011522082.1:p.Arg217= | |
NM_000697.3:c.294C>G (ALOX12) MANE Select | NP_000688.2:p.Arg98= |