Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983376T>G , CM000678.2:g.56983376T>G | GRCh38 |
| NC_000016.9:g.57017288T>G , CM000678.1:g.57017288T>G | GRCh37 |
| NC_000016.8:g.55574789T>G | NCBI36 |
| NG_008952.1:g.26454T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000200676.8:c.1372T>G MANE Select | ENSP00000200676.3:p.Phe458Val | |
| ENST00000650358.1:n.1770T>G | ||
| ENST00000200676.7:c.1372T>G | ENSP00000200676.3:p.Phe458Val | |
| ENST00000379780.6:c.1192T>G | ENSP00000369106.2:p.Phe398Val | |
| ENST00000566128.1:c.1177T>G | ENSP00000456276.1:p.Phe393Val | |
| NM_000078.2:c.1372T>G | NP_000069.2:p.Phe458Val | |
| NM_001286085.1:c.1192T>G | NP_001273014.1:p.Phe398Val | |
| NM_000078.3:c.1372T>G MANE Select | NP_000069.2:p.Phe458Val | |
| NM_001286085.2:c.1192T>G | NP_001273014.1:p.Phe398Val |