Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178014318G>C , CM000664.2:g.178014318G>C | GRCh38 |
| NC_000002.11:g.178879045G>C , CM000664.1:g.178879045G>C | GRCh37 |
| NC_000002.10:g.178587291G>C | NCBI36 |
| NG_012168.1:g.99022C>G | |
| NG_012168.2:g.99022C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286063.11:c.1055C>G MANE Select | ENSP00000286063.5:p.Thr352Ser | |
| ENST00000286063.10:c.1055C>G | ENSP00000286063.5:p.Thr352Ser | |
| ENST00000358450.8:c.305C>G | ENSP00000351232.4:p.Thr102Ser | |
| NM_001077197.1:c.305C>G | NP_001070665.1:p.Thr102Ser | |
| NM_016953.3:c.1055C>G | NP_058649.3:p.Thr352Ser | |
| NM_016953.4:c.1055C>G MANE Select | NP_058649.3:p.Thr352Ser | |
| NM_001077197.2:c.305C>G | NP_001070665.1:p.Thr102Ser |