HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734195_4734196del , CM000679.2:g.4734195_4734196del | GRCh38 |
NC_000017.10:g.4637490_4637491del , CM000679.1:g.4637490_4637491del | GRCh37 |
NC_000017.9:g.4584239_4584240del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*309_*310del MANE Select | ENSP00000293778.7:n.*309_*310del | |
ENST00000293778.10:c.*309_*310del | ENSP00000293778.6:n.*309_*310del | |
ENST00000576153.5:n.865_866del | ||
NM_022059.3:c.*309_*310del | NP_071342.2:n.*309_*310del | |
NM_022059.4:c.*309_*310del | NP_071342.2:n.*309_*310del | |
NM_001386809.1:c.*309_*310del MANE Select | NP_001373738.1:n.*309_*310del |