Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912547C>A , CM000674.2:g.4912547C>A | GRCh38 |
| NC_000012.11:g.5021713C>A , CM000674.1:g.5021713C>A | GRCh37 |
| NC_000012.10:g.4891974C>A | NCBI36 |
| NG_011815.1:g.7641C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.1169C>A MANE Select | ENSP00000371985.3:p.Ser390Tyr | |
| ENST00000543874.3:n.105+2075C>A | ||
| ENST00000639306.1:c.1007C>A | ENSP00000492506.1:p.Ser336Tyr | |
| ENST00000639680.1:c.76+281C>A | ||
| ENST00000382545.3:c.1169C>A | ENSP00000371985.3:p.Ser390Tyr | |
| ENST00000541095.1:n.105+2075C>A | ||
| ENST00000543874.2:n.96+2075C>A | ||
| NM_000217.2:c.1169C>A | NP_000208.2:p.Ser390Tyr | |
| NM_000217.3:c.1169C>A MANE Select | NP_000208.2:p.Ser390Tyr |