Linked Data
gnomAD v4:
1-193251992-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193251992G>T , CM000663.2:g.193251992G>T | GRCh38 |
| NC_000001.10:g.193221122G>T , CM000663.1:g.193221122G>T | GRCh37 |
| NC_000001.9:g.191487745G>T | NCBI36 |
| NG_012691.1:g.135035G>T , LRG_507:g.135035G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.*1280G>T MANE Select | ENSP00000356405.4:n.*1280G>T | |
| ENST00000635846.1:c.*1280G>T | ENSP00000490035.1:n.*1280G>T | |
| ENST00000643006.1:c.*1786G>T | ENSP00000496633.1:n.*1786G>T | |
| ENST00000367435.3:c.*1280G>T | ENSP00000356405.3:n.*1280G>T | |
| NM_024529.4:c.*1280G>T , LRG_507t1:c.*1280G>T | NP_078805.3:n.*1280G>T | |
| NM_024529.5:c.*1280G>T MANE Select | NP_078805.3:n.*1280G>T |