Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74750132G>T , CM000677.2:g.74750132G>T | GRCh38 |
| NC_000015.9:g.75042473G>T , CM000677.1:g.75042473G>T | GRCh37 |
| NC_000015.8:g.72829526G>T | NCBI36 |
| NG_008431.1:g.32591G>T | |
| NG_008431.2:g.32591G>T | |
| NG_061543.1:g.6288G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.394G>T MANE Select | ENSP00000342007.4:p.Val132Leu | |
| ENST00000343932.4:c.394G>T | ENSP00000342007.4:p.Val132Leu | |
| NM_000761.4:c.394G>T | NP_000752.2:p.Val132Leu | |
| NM_000761.5:c.394G>T MANE Select | NP_000752.2:p.Val132Leu |