Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21000994T>G , CM000676.2:g.21000994T>G | GRCh38 |
| NC_000014.8:g.21469153T>G , CM000676.1:g.21469153T>G | GRCh37 |
| NC_000014.7:g.20538993T>G | NCBI36 |
| NG_017065.1:g.6740T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014579.4:c.345T>G MANE Select | NP_055394.2:p.Phe115Leu |
| ENST00000298681.5:c.345T>G MANE Select | ENSP00000298681.4:p.Phe115Leu |
| NM_001256588.1:c.*82T>G | NP_001243517.1:n.*82T>G |
| NM_001256588.2:c.*82T>G | NP_001243517.1:n.*82T>G |
| NM_014579.3:c.345T>G | NP_055394.2:p.Phe115Leu |
| ENST00000298681.4:c.345T>G | ENSP00000298681.4:p.Phe115Leu |
| ENST00000554422.5:c.*82T>G | ENSP00000452568.1:n.*82T>G |