Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.43067915T>A , CM000677.2:g.43067915T>A | GRCh38 |
| NC_000015.9:g.43360113T>A , CM000677.1:g.43360113T>A | GRCh37 |
| NC_000015.8:g.41147405T>A | NCBI36 |
| NG_012182.1:g.43174A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290650.9:c.781A>T MANE Select | ENSP00000290650.4:p.Thr261Ser | |
| ENST00000290650.8:c.781A>T | ENSP00000290650.4:p.Thr261Ser | |
| ENST00000546274.6:c.781A>T | ENSP00000477932.1:p.Thr261Ser | |
| ENST00000563239.1:c.*202+2984A>T | ENSP00000456502.1:n.*202+2984A>T | |
| NM_174916.2:c.781A>T | NP_777576.1:p.Thr261Ser | |
| NM_174916.3:c.781A>T MANE Select | NP_777576.1:p.Thr261Ser |