Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911871C>A , CM000674.2:g.4911871C>A | GRCh38 |
| NC_000012.11:g.5021037C>A , CM000674.1:g.5021037C>A | GRCh37 |
| NC_000012.10:g.4891298C>A | NCBI36 |
| NG_011815.1:g.6965C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.493C>A MANE Select | ENSP00000371985.3:p.Pro165Thr | |
| ENST00000543874.3:n.105+1399C>A | ||
| ENST00000639306.1:c.331C>A | ENSP00000492506.1:p.Pro111Thr | |
| ENST00000382545.3:c.493C>A | ENSP00000371985.3:p.Pro165Thr | |
| ENST00000541095.1:n.105+1399C>A | ||
| ENST00000543874.2:n.96+1399C>A | ||
| NM_000217.2:c.493C>A | NP_000208.2:p.Pro165Thr | |
| NM_000217.3:c.493C>A MANE Select | NP_000208.2:p.Pro165Thr |