HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461896C>T , CM000672.2:g.122461896C>T | GRCh38 |
NC_000010.10:g.124221412C>T , CM000672.1:g.124221412C>T | GRCh37 |
NC_000010.9:g.124211402C>T | NCBI36 |
NG_011554.1:g.5372C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.244C>T MANE Select | ENSP00000357980.3:p.Pro82Ser | |
ENST00000648167.1:c.154+3187C>T | ENSP00000498033.1:n.154+3187C>T | |
ENST00000368984.7:c.244C>T | ENSP00000357980.3:p.Pro82Ser | |
NM_002775.4:c.244C>T | NP_002766.1:p.Pro82Ser | |
NM_002775.5:c.244C>T MANE Select | NP_002766.1:p.Pro82Ser |