HGVS | Genome Assembly |
---|---|
NC_000008.11:g.142912547G= , CM000670.2:g.142912547G= | GRCh38 |
NC_000008.10:g.143993963G= , CM000670.1:g.143993963G= | GRCh37 |
NC_000008.9:g.143990965G= | NCBI36 |
NG_008374.1:g.10297C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000323110.2:c.1381C= (CYP11B2) MANE Select | ENSP00000325822.2:p.Leu461= | |
ENST00000522728.5:c.182-1416G= (GML) | ENSP00000430799.1:n.182-1416G= | |
NM_000498.3:c.1381C= (CYP11B2) MANE Select | NP_000489.3:p.Leu461= | |
XM_011516877.1:c.1528C= (CYP11B2) | XP_011515179.1:p.Leu510= | |
XM_011516878.1:c.1459C= (CYP11B2) | XP_011515180.1:p.Leu487= | |
XM_011516879.1:c.1450C= (CYP11B2) | XP_011515181.1:p.Leu484= | |
XM_011516970.1:c.215-1416G= (GML) | XP_011515272.1:n.215-1416G= |