HGVS | Genome Assembly |
---|---|
NC_000015.10:g.84840563T>A , CM000677.2:g.84840563T>A | GRCh38 |
NC_000015.9:g.85383794T>A , CM000677.1:g.85383794T>A | GRCh37 |
NC_000015.8:g.83184798T>A | NCBI36 |
NG_054748.1:g.28933T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258888.6:c.1284T>A MANE Select | ENSP00000258888.6:p.Pro428= | |
ENST00000258888.5:c.1890T>A | ENSP00000258888.5:p.Pro630= | |
NM_020778.4:c.1890T>A | NP_065829.3:p.Pro630= | |
NM_020778.5:c.1284T>A MANE Select | NP_065829.4:p.Pro428= |