Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102527881T>A , CM000673.2:g.102527881T>A | GRCh38 |
| NC_000011.9:g.102398612T>A , CM000673.1:g.102398612T>A | GRCh37 |
| NC_000011.8:g.101903822T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260227.5:c.211A>T MANE Select | ENSP00000260227.4:p.Thr71Ser | |
| ENST00000260227.4:c.211A>T | ENSP00000260227.4:p.Thr71Ser | |
| ENST00000531200.1:n.258A>T | ||
| ENST00000533366.5:n.261A>T | ||
| NM_002423.3:c.211A>T | NP_002414.1:p.Thr71Ser | |
| NM_002423.4:c.211A>T | NP_002414.1:p.Thr71Ser | |
| NM_002423.5:c.211A>T MANE Select | NP_002414.1:p.Thr71Ser |