Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.142914735A>T , CM000670.2:g.142914735A>T | GRCh38 |
| NC_000008.10:g.143996151A>T , CM000670.1:g.143996151A>T | GRCh37 |
| NC_000008.9:g.143993153A>T | NCBI36 |
| NG_008374.1:g.8109T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323110.2:c.769T>A (CYP11B2) MANE Select | ENSP00000325822.2:p.Phe257Ile | |
| ENST00000522728.5:c.264+690A>T (GML) | ENSP00000430799.1:n.264+690A>T | |
| NM_000498.3:c.769T>A (CYP11B2) MANE Select | NP_000489.3:p.Phe257Ile | |
| XM_011516877.1:c.847T>A (CYP11B2) | XP_011515179.1:p.Phe283Ile | |
| XM_011516878.1:c.847T>A (CYP11B2) | XP_011515180.1:p.Phe283Ile | |
| XM_011516879.1:c.769T>A (CYP11B2) | XP_011515181.1:p.Phe257Ile | |
| XM_011516970.1:c.297+690A>T (GML) | XP_011515272.1:n.297+690A>T |