Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766155A>C , CM000674.2:g.57766155A>C | GRCh38 |
| NC_000012.11:g.58159938A>C , CM000674.1:g.58159938A>C | GRCh37 |
| NC_000012.10:g.56446205A>C | NCBI36 |
| NG_007076.1:g.6039T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.150T>G | ||
| ENST00000713544.1:c.238T>G | ENSP00000518840.1:p.Phe80Val | |
| ENST00000713545.1:c.238T>G | ENSP00000518841.1:p.Phe80Val | |
| ENST00000228606.9:c.238T>G MANE Select | ENSP00000228606.4:p.Phe80Val | |
| ENST00000228606.8:c.238T>G | ENSP00000228606.4:p.Phe80Val | |
| ENST00000546496.1:n.66T>G | ||
| ENST00000546609.1:c.150T>G | ||
| ENST00000547344.5:n.292T>G | ||
| ENST00000552186.1:n.357T>G | ||
| NM_000785.3:c.238T>G | NP_000776.1:p.Phe80Val | |
| NM_000785.4:c.238T>G MANE Select | NP_000776.1:p.Phe80Val |