HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7001573G= , CM000679.2:g.7001573G= | GRCh38 |
NC_000017.10:g.6904892G= , CM000679.1:g.6904892G= | GRCh37 |
NC_000017.9:g.6845616G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.952-29G= (ALOX12) MANE Select | ENSP00000251535.6:n.952-29G= | |
ENST00000251535.10:c.952-29G= (ALOX12) | ENSP00000251535.6:n.952-29G= | |
NM_000697.2:c.952-29G= (ALOX12) | NP_000688.2:n.952-29G= | |
NR_040089.1:n.233+8223C= (ALOX12-AS1) | ||
XM_011523780.1:c.1102-29G= (ALOX12) | XP_011522082.1:n.1102-29G= | |
XM_011523780.2:c.1102-29G= (ALOX12) | XP_011522082.1:n.1102-29G= | |
NM_000697.3:c.952-29G= (ALOX12) MANE Select | NP_000688.2:n.952-29G= |