Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14978120T>G , CM000674.2:g.14978120T>G | GRCh38 |
| NC_000012.11:g.15131054T>G , CM000674.1:g.15131054T>G | GRCh37 |
| NC_000012.10:g.15022321T>G | NCBI36 |
| NG_016859.1:g.10099T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266395.3:c.108T>G MANE Select | ENSP00000266395.2:p.Ser36Arg | |
| ENST00000266395.2:c.108T>G | ENSP00000266395.2:p.Ser36Arg | |
| NM_006205.2:c.108T>G | NP_006196.1:p.Ser36Arg | |
| XR_931376.1:n.175+11367A>C | ||
| XM_017019431.2:c.108T>G | XP_016874920.1:p.Ser36Arg | |
| XR_931376.2:n.389+11367A>C | ||
| NM_006205.3:c.108T>G MANE Select | NP_006196.1:p.Ser36Arg |