Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75005911A>T , CM000676.2:g.75005911A>T | GRCh38 |
| NC_000014.8:g.75472614A>T , CM000676.1:g.75472614A>T | GRCh37 |
| NC_000014.7:g.74542367A>T | NCBI36 |
| NG_013333.1:g.8003A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.643A>T MANE Select | ENSP00000266126.5:p.Thr215Ser | |
| ENST00000266126.9:c.643A>T | ENSP00000266126.5:p.Thr215Ser | |
| ENST00000553401.5:c.641A>T | ENSP00000451681.1:n.641A>T | |
| ENST00000554748.2:c.7A>T | ENSP00000452582.2:p.Thr3Ser | |
| ENST00000556028.5:c.612A>T | ENSP00000452311.1:p.Gln204His | |
| NM_014239.3:c.643A>T | NP_055054.1:p.Thr215Ser | |
| NM_014239.4:c.643A>T MANE Select | NP_055054.1:p.Thr215Ser |