Linked Data
ClinVar Variation Id:
362176
dbSNP Id:
rs61763990
gnomAD v2:
8-143992607-C-T
gnomAD v3:
8-142911191-C-T
gnomAD v4:
8-142911191-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.142911191C>T , CM000670.2:g.142911191C>T | GRCh38 |
| NC_000008.10:g.143992607C>T , CM000670.1:g.143992607C>T | GRCh37 |
| NC_000008.9:g.143989609C>T | NCBI36 |
| NG_008374.1:g.11653G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323110.2:c.*789G>A (CYP11B2) MANE Select | ENSP00000325822.2:n.*789G>A | |
| ENST00000522728.5:c.182-2772C>T (GML) | ENSP00000430799.1:n.182-2772C>T | |
| NM_000498.3:c.*789G>A (CYP11B2) MANE Select | NP_000489.3:n.*789G>A | |
| XM_011516877.1:c.*789G>A (CYP11B2) | XP_011515179.1:n.*789G>A | |
| XM_011516878.1:c.*789G>A (CYP11B2) | XP_011515180.1:n.*789G>A | |
| XM_011516879.1:c.*789G>A (CYP11B2) | XP_011515181.1:n.*789G>A | |
| XM_011516970.1:c.215-2772C>T (GML) | XP_011515272.1:n.215-2772C>T |