Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7455332C>T , CM000679.2:g.7455332C>T | GRCh38 |
| NC_000017.10:g.7358651C>T , CM000679.1:g.7358651C>T | GRCh37 |
| NC_000017.9:g.7299375C>T | NCBI36 |
| NG_008026.1:g.15246C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.1093C>T MANE Select | ENSP00000304290.2:p.Pro365Ser | |
| ENST00000306071.6:c.1093C>T | ENSP00000304290.2:p.Pro365Ser | |
| ENST00000536404.6:c.877C>T | ENSP00000439209.2:p.Pro293Ser | |
| ENST00000570557.5:c.756C>T | ||
| ENST00000573209.1:n.2037C>T | ||
| ENST00000576360.1:c.730C>T | ENSP00000459092.1:p.Pro244Ser | |
| NM_000747.2:c.1093C>T | NP_000738.2:p.Pro365Ser | |
| NM_000747.3:c.1093C>T MANE Select | NP_000738.2:p.Pro365Ser |