HGVS | Genome Assembly |
---|---|
NC_000008.11:g.142912555G= , CM000670.2:g.142912555G= | GRCh38 |
NC_000008.10:g.143993971G= , CM000670.1:g.143993971G= | GRCh37 |
NC_000008.9:g.143990973G= | NCBI36 |
NG_008374.1:g.10289C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000323110.2:c.1373C= (CYP11B2) MANE Select | ENSP00000325822.2:p.Ala458= | |
ENST00000522728.5:c.182-1408G= (GML) | ENSP00000430799.1:n.182-1408G= | |
NM_000498.3:c.1373C= (CYP11B2) MANE Select | NP_000489.3:p.Ala458= | |
XM_011516877.1:c.1520C= (CYP11B2) | XP_011515179.1:p.Ala507= | |
XM_011516878.1:c.1451C= (CYP11B2) | XP_011515180.1:p.Ala484= | |
XM_011516879.1:c.1442C= (CYP11B2) | XP_011515181.1:p.Ala481= | |
XM_011516970.1:c.215-1408G= (GML) | XP_011515272.1:n.215-1408G= |