Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221630A>T , CM000671.2:g.99221630A>T | GRCh38 |
| NC_000009.11:g.101983912A>T , CM000671.1:g.101983912A>T | GRCh37 |
| NC_000009.10:g.101023733A>T | NCBI36 |
| NG_008928.1:g.5335T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476832.2:c.265T>A MANE Select | ENSP00000417764.1:p.Cys89Ser | |
| ENST00000238477.5:c.265T>A | ENSP00000432675.2:p.Cys89Ser | |
| ENST00000476832.1:c.265T>A | ENSP00000417764.1:p.Cys89Ser | |
| NM_033087.3:c.265T>A | NP_149078.1:p.Cys89Ser | |
| NR_024532.1:n.335T>A | ||
| NM_033087.4:c.265T>A MANE Select | NP_149078.1:p.Cys89Ser | |
| NR_024532.2:n.313T>A |