HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6997021G>C , CM000679.2:g.6997021G>C | GRCh38 |
NC_000017.10:g.6900340G>C , CM000679.1:g.6900340G>C | GRCh37 |
NC_000017.9:g.6841064G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.331G>C (ALOX12) MANE Select | ENSP00000251535.6:p.Gly111Arg | |
ENST00000251535.10:c.331G>C (ALOX12) | ENSP00000251535.6:p.Gly111Arg | |
ENST00000480801.1:c.40G>C (ALOX12) | ENSP00000467033.1:p.Gly14Arg | |
NM_000697.2:c.331G>C (ALOX12) | NP_000688.2:p.Gly111Arg | |
NR_040089.1:n.234-11481C>G (ALOX12-AS1) | ||
XM_011523780.1:c.688G>C (ALOX12) | XP_011522082.1:p.Gly230Arg | |
XM_011523780.2:c.688G>C (ALOX12) | XP_011522082.1:p.Gly230Arg | |
NM_000697.3:c.331G>C (ALOX12) MANE Select | NP_000688.2:p.Gly111Arg |