HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122506793A>T , CM000672.2:g.122506793A>T | GRCh38 |
NC_000010.10:g.124266309A>T , CM000672.1:g.124266309A>T | GRCh37 |
NC_000010.9:g.124256299A>T | NCBI36 |
NG_011554.1:g.50269A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.880A>T MANE Select | ENSP00000357980.3:p.Thr294Ser | |
ENST00000648167.1:c.562A>T | ENSP00000498033.1:p.Thr188Ser | |
ENST00000368984.7:c.880A>T | ENSP00000357980.3:p.Thr294Ser | |
ENST00000420892.1:c.103A>T | ENSP00000412676.1:p.Thr35Ser | |
NM_002775.4:c.880A>T | NP_002766.1:p.Thr294Ser | |
NM_002775.5:c.880A>T MANE Select | NP_002766.1:p.Thr294Ser |