Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165069092G>C , CM000665.2:g.165069092G>C | GRCh38 |
| NC_000003.11:g.164786880G>C , CM000665.1:g.164786880G>C | GRCh37 |
| NC_000003.10:g.166269574G>C | NCBI36 |
| NG_017043.1:g.14404C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264382.8:c.359C>G MANE Select | ENSP00000264382.3:p.Thr120Arg | |
| ENST00000264382.7:c.359C>G | ENSP00000264382.3:p.Thr120Arg | |
| ENST00000476593.1:c.*234C>G | ENSP00000419450.1:n.*234C>G | |
| NM_001041.3:c.359C>G | NP_001032.2:p.Thr120Arg | |
| XM_011513078.1:c.260C>G | XP_011511380.1:p.Thr87Arg | |
| XM_011513078.2:c.260C>G | XP_011511380.1:p.Thr87Arg | |
| NM_001041.4:c.359C>G MANE Select | NP_001032.2:p.Thr120Arg |