Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45766515A>T , CM000681.2:g.45766515A>T | GRCh38 |
| NC_000019.9:g.46269773A>T , CM000681.1:g.46269773A>T | GRCh37 |
| NC_000019.8:g.50961613A>T | NCBI36 |
| NG_012745.1:g.7725T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317578.7:c.1444T>A MANE Select | ENSP00000316842.4:p.Ser482Thr | |
| ENST00000317578.6:c.1444T>A | ENSP00000316842.4:p.Ser482Thr | |
| ENST00000560160.1:c.587-404T>A | ||
| ENST00000560168.1:c.*632T>A | ENSP00000453189.2:n.*632T>A | |
| ENST00000622857.1:c.16-553T>A | ENSP00000481365.1:n.16-553T>A | |
| NM_175875.4:c.1444T>A | NP_787071.2:p.Ser482Thr | |
| NM_175875.5:c.1444T>A MANE Select | NP_787071.3:p.Ser482Thr |