Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.142912557C= , CM000670.2:g.142912557C= | GRCh38 |
| NC_000008.10:g.143993973C= , CM000670.1:g.143993973C= | GRCh37 |
| NC_000008.9:g.143990975C= | NCBI36 |
| NG_008374.1:g.10287G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000323110.2:c.1371G= (CYP11B2) MANE Select | ENSP00000325822.2:p.Glu457= | |
| ENST00000522728.5:c.182-1406C= (GML) | ENSP00000430799.1:n.182-1406C= | |
| NM_000498.3:c.1371G= (CYP11B2) MANE Select | NP_000489.3:p.Glu457= | |
| XM_011516877.1:c.1518G= (CYP11B2) | XP_011515179.1:p.Glu506= | |
| XM_011516878.1:c.1449G= (CYP11B2) | XP_011515180.1:p.Glu483= | |
| XM_011516879.1:c.1440G= (CYP11B2) | XP_011515181.1:p.Glu480= | |
| XM_011516970.1:c.215-1406C= (GML) | XP_011515272.1:n.215-1406C= |