Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52516698T>C , CM000674.2:g.52516698T>C | GRCh38 |
| NC_000012.11:g.52910482T>C , CM000674.1:g.52910482T>C | GRCh37 |
| NC_000012.10:g.51196749T>C | NCBI36 |
| NG_008297.1:g.8762A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.1378A>G MANE Select | ENSP00000252242.4:p.Lys460Glu | |
| ENST00000252242.8:c.1378A>G | ENSP00000252242.4:p.Lys460Glu | |
| ENST00000547890.5:n.756A>G | ||
| ENST00000548409.5:c.500A>G | ||
| ENST00000549511.5:n.585A>G | ||
| ENST00000552629.5:n.1476A>G | ||
| NM_000424.3:c.1378A>G | NP_000415.2:p.Lys460Glu | |
| NM_000424.4:c.1378A>G MANE Select | NP_000415.2:p.Lys460Glu |