Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911373A>G , CM000679.2:g.42911373A>G | GRCh38 |
| NC_000017.10:g.41063390A>G , CM000679.1:g.41063390A>G | GRCh37 |
| NC_000017.9:g.38316916A>G | NCBI36 |
| NG_011808.1:g.15576A>G , LRG_147:g.15576A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.1021A>G MANE Select | ENSP00000253801.1:p.Ile341Val | |
| ENST00000253801.6:c.1021A>G | ENSP00000253801.1:p.Ile341Val | |
| ENST00000585489.1:c.*413A>G | ENSP00000466202.1:n.*413A>G | |
| NM_000151.3:c.1021A>G | NP_000142.2:p.Ile341Val | |
| NM_001270397.1:c.*413A>G | NP_001257326.1:n.*413A>G | |
| NM_000151.4:c.1021A>G MANE Select | NP_000142.2:p.Ile341Val | |
| NM_001270397.2:c.*413A>G | NP_001257326.1:n.*413A>G |