Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122508751C>G , CM000672.2:g.122508751C>G | GRCh38 |
| NC_000010.10:g.124268267C>G , CM000672.1:g.124268267C>G | GRCh37 |
| NC_000010.9:g.124258257C>G | NCBI36 |
| NG_011554.1:g.52227C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000368984.8:c.1101C>G MANE Select | ENSP00000357980.3:p.Ser367= | |
| ENST00000648167.1:c.783C>G | ENSP00000498033.1:p.Ser261= | |
| ENST00000368984.7:c.1101C>G | ENSP00000357980.3:p.Ser367= | |
| ENST00000420892.1:c.324C>G | ENSP00000412676.1:p.Ser108= | |
| NM_002775.4:c.1101C>G | NP_002766.1:p.Ser367= | |
| NM_002775.5:c.1101C>G MANE Select | NP_002766.1:p.Ser367= |