Linked Data
dbSNP Id:
rs2097486369
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122472111T>A , CM000672.2:g.122472111T>A | GRCh38 |
| NC_000010.10:g.124231627T>A , CM000672.1:g.124231627T>A | GRCh37 |
| NC_000010.9:g.124221617T>A | NCBI36 |
| NG_011554.1:g.15587T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.472+9987T>A MANE Select | ENSP00000357980.3:n.472+9987T>A | |
| ENST00000648167.1:c.154+13402T>A | ENSP00000498033.1:n.154+13402T>A | |
| ENST00000368984.7:c.472+9987T>A | ENSP00000357980.3:n.472+9987T>A | |
| NM_002775.4:c.472+9987T>A | NP_002766.1:n.472+9987T>A | |
| NM_002775.5:c.472+9987T>A MANE Select | NP_002766.1:n.472+9987T>A |