Linked Data
gnomAD v4:
12-114670332-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114670332C>T , CM000674.2:g.114670332C>T | GRCh38 |
| NC_000012.11:g.115108137C>T , CM000674.1:g.115108137C>T | GRCh37 |
| NC_000012.10:g.113592520C>T | NCBI36 |
| NG_008315.1:g.18833G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349155.7:c.*1509G>A MANE Select | ENSP00000257567.2:n.*1509G>A | |
| ENST00000257566.7:c.*1509G>A | ENSP00000257566.3:n.*1509G>A | |
| ENST00000349155.6:c.*1509G>A | ENSP00000257567.2:n.*1509G>A | |
| NM_005996.3:c.*1509G>A | NP_005987.3:n.*1509G>A | |
| NM_016569.3:c.*1509G>A | NP_057653.3:n.*1509G>A | |
| NM_005996.4:c.*1509G>A MANE Select | NP_005987.3:n.*1509G>A | |
| NM_016569.4:c.*1509G>A | NP_057653.3:n.*1509G>A |