Linked Data
ClinVar Variation Id:
2850392
ClinVar RCV Id:
RCV003688289
MyVariant Identifiers:
chr8:g.143957265A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.142875849A>G , CM000670.2:g.142875849A>G | GRCh38 |
| NC_000008.10:g.143957265A>G , CM000670.1:g.143957265A>G | GRCh37 |
| NC_000008.9:g.143954267A>G | NCBI36 |
| NG_007954.1:g.8972T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292427.10:c.984T>C (CYP11B1) MANE Select | ENSP00000292427.5:p.Phe328= | |
| ENST00000292427.8:c.984T>C (CYP11B1) | ENSP00000292427.4:p.Phe328= | |
| ENST00000314111.4:n.1379T>C (CYP11B1) | ||
| ENST00000377675.3:c.1197T>C (CYP11B1) | ENSP00000366903.3:p.Phe399= | |
| ENST00000517471.5:c.984T>C (CYP11B1) | ENSP00000428043.1:p.Phe328= | |
| ENST00000522728.5:c.181+34624A>G (GML) | ENSP00000430799.1:n.181+34624A>G | |
| NM_000497.3:c.984T>C (CYP11B1) | NP_000488.3:p.Phe328= | |
| NM_001026213.1:c.984T>C (CYP11B1) | NP_001021384.1:p.Phe328= | |
| XM_011516870.1:c.1062T>C (CYP11B1) | XP_011515172.1:p.Phe354= | |
| XM_011516871.1:c.1062T>C (CYP11B1) | XP_011515173.1:p.Phe354= | |
| XM_011516872.1:c.984T>C (CYP11B1) | XP_011515174.1:p.Phe328= | |
| XM_011516873.1:c.1062T>C (CYP11B1) | XP_011515175.1:p.Phe354= | |
| XM_011516874.1:c.1062T>C (CYP11B1) | XP_011515176.1:p.Phe354= | |
| XM_011516875.1:c.801T>C (CYP11B1) | XP_011515177.1:p.Phe267= | |
| XM_011516876.1:c.1062T>C (CYP11B1) | XP_011515178.1:p.Phe354= | |
| XM_011516970.1:c.214+34624A>G (GML) | XP_011515272.1:n.214+34624A>G | |
| NM_000497.4:c.984T>C (CYP11B1) MANE Select | NP_000488.3:p.Phe328= |