Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911316T>G , CM000679.2:g.42911316T>G | GRCh38 |
| NC_000017.10:g.41063333T>G , CM000679.1:g.41063333T>G | GRCh37 |
| NC_000017.9:g.38316859T>G | NCBI36 |
| NG_011808.1:g.15519T>G , LRG_147:g.15519T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000151.4:c.964T>G MANE Select | NP_000142.2:p.Phe322Val |
| ENST00000253801.7:c.964T>G MANE Select | ENSP00000253801.1:p.Phe322Val |
| NM_000151.3:c.964T>G | NP_000142.2:p.Phe322Val |
| NM_001270397.1:c.*356T>G | NP_001257326.1:n.*356T>G |
| NM_001270397.2:c.*356T>G | NP_001257326.1:n.*356T>G |
| ENST00000253801.6:c.964T>G | ENSP00000253801.1:p.Phe322Val |
| ENST00000585489.1:c.*356T>G | ENSP00000466202.1:n.*356T>G |
| ENST00000592383.5:c.*356T>G | ENSP00000465958.1:n.*356T>G |