HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6997033C>G , CM000679.2:g.6997033C>G | GRCh38 |
NC_000017.10:g.6900352C>G , CM000679.1:g.6900352C>G | GRCh37 |
NC_000017.9:g.6841076C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.337+6C>G (ALOX12) MANE Select | ENSP00000251535.6:n.337+6C>G | |
ENST00000251535.10:c.337+6C>G (ALOX12) | ENSP00000251535.6:n.337+6C>G | |
ENST00000480801.1:c.46+6C>G (ALOX12) | ENSP00000467033.1:n.46+6C>G | |
NM_000697.2:c.337+6C>G (ALOX12) | NP_000688.2:n.337+6C>G | |
NR_040089.1:n.234-11493G>C (ALOX12-AS1) | ||
XM_011523780.1:c.694+6C>G (ALOX12) | XP_011522082.1:n.694+6C>G | |
XM_011523780.2:c.694+6C>G (ALOX12) | XP_011522082.1:n.694+6C>G | |
NM_000697.3:c.337+6C>G (ALOX12) MANE Select | NP_000688.2:n.337+6C>G |