Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52519881C>A , CM000674.2:g.52519881C>A | GRCh38 |
| NC_000012.11:g.52913665C>A , CM000674.1:g.52913665C>A | GRCh37 |
| NC_000012.10:g.51199932C>A | NCBI36 |
| NG_008297.1:g.5579G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.416G>T MANE Select | ENSP00000252242.4:p.Gly139Val | |
| ENST00000252242.8:c.416G>T | ENSP00000252242.4:p.Gly139Val | |
| ENST00000549420.1:c.86G>T | ENSP00000447209.1:p.Gly29Val | |
| ENST00000551275.1:c.311G>T | ENSP00000448041.1:p.Gly104Val | |
| ENST00000552629.5:n.514G>T | ||
| NM_000424.3:c.416G>T | NP_000415.2:p.Gly139Val | |
| NM_000424.4:c.416G>T MANE Select | NP_000415.2:p.Gly139Val |