Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1986017T>A , CM000678.2:g.1986017T>A | GRCh38 |
| NC_000016.9:g.2036018T>A , CM000678.1:g.2036018T>A | GRCh37 |
| NC_000016.8:g.1976019T>A | NCBI36 |
| NG_016288.1:g.6869T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.382T>A | ENSP00000455885.1:p.Ser128Thr | |
| ENST00000248114.7:c.607T>A MANE Select | ENSP00000248114.6:p.Ser203Thr | |
| ENST00000248114.6:c.607T>A | ENSP00000248114.6:p.Ser203Thr | |
| ENST00000565658.1:n.764T>A | ||
| ENST00000567719.1:c.382T>A | ENSP00000455885.1:p.Ser128Thr | |
| ENST00000569451.1:c.*80T>A | ENSP00000456432.1:n.*80T>A | |
| NM_005262.2:c.607T>A | NP_005253.3:p.Ser203Thr | |
| NM_005262.3:c.607T>A MANE Select | NP_005253.3:p.Ser203Thr |