Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92637466T>C , CM000672.2:g.92637466T>C | GRCh38 |
| NC_000010.10:g.94397223T>C , CM000672.1:g.94397223T>C | GRCh37 |
| NC_000010.9:g.94387203T>C | NCBI36 |
| NG_032580.1:g.49399T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.2081T>C MANE Select | ENSP00000260731.3:p.Ile694Thr | |
| ENST00000676621.1:c.*599T>C | ENSP00000503639.1:n.*599T>C | |
| ENST00000676647.1:c.1874T>C | ENSP00000503394.1:p.Ile625Thr | |
| ENST00000676757.1:c.1874T>C | ENSP00000504289.1:p.Ile625Thr | |
| ENST00000677720.1:c.*55T>C | ENSP00000504840.1:n.*55T>C | |
| ENST00000260731.4:c.2081T>C | ENSP00000260731.3:p.Ile694Thr | |
| NM_004523.3:c.2081T>C | NP_004514.2:p.Ile694Thr | |
| NM_004523.4:c.2081T>C MANE Select | NP_004514.2:p.Ile694Thr |