Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763700G>A , CM000674.2:g.57763700G>A | GRCh38 |
| NC_000012.11:g.58157483G>A , CM000674.1:g.58157483G>A | GRCh37 |
| NC_000012.10:g.56443750G>A | NCBI36 |
| NG_007076.1:g.8494C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000713544.1:c.1405C>T | ENSP00000518840.1:p.Pro469Ser | |
| ENST00000713545.1:c.*329C>T | ENSP00000518841.1:n.*329C>T | |
| ENST00000228606.9:c.1324C>T MANE Select | ENSP00000228606.4:p.Pro442Ser | |
| ENST00000228606.8:c.1324C>T | ENSP00000228606.4:p.Pro442Ser | |
| ENST00000547344.5:n.1463C>T | ||
| NM_000785.3:c.1324C>T | NP_000776.1:p.Pro442Ser | |
| NM_000785.4:c.1324C>T MANE Select | NP_000776.1:p.Pro442Ser |