Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215888961A>C , CM000663.2:g.215888961A>C | GRCh38 |
| NC_000001.10:g.216062303A>C , CM000663.1:g.216062303A>C | GRCh37 |
| NC_000001.9:g.214128926A>C | NCBI36 |
| NG_009497.1:g.539436T>G | |
| NG_009497.2:g.539488T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.7688T>G MANE Select | ENSP00000305941.3:p.Ile2563Ser | |
| ENST00000674083.1:c.7688T>G | ENSP00000501296.1:p.Ile2563Ser | |
| ENST00000307340.7:c.7688T>G | ENSP00000305941.3:p.Ile2563Ser | |
| NM_206933.2:c.7688T>G | NP_996816.2:p.Ile2563Ser | |
| NM_206933.3:c.7688T>G | NP_996816.2:p.Ile2563Ser | |
| NM_206933.4:c.7688T>G MANE Select | NP_996816.3:p.Ile2563Ser |