HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631143_4631144del , CM000679.2:g.4631143_4631144del | GRCh38 |
NC_000017.10:g.4534438_4534439del , CM000679.1:g.4534438_4534439del | GRCh37 |
NC_000017.9:g.4481187_4481188del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.*456_*457del MANE Select | ENSP00000293761.3:n.*456_*457del | |
ENST00000293761.7:c.*456_*457del | ENSP00000293761.3:n.*456_*457del | |
ENST00000570836.5:c.*456_*457del | ENSP00000458832.1:n.*456_*457del | |
NM_001140.3:c.*456_*457del | NP_001131.3:n.*456_*457del | |
NM_001140.4:c.*456_*457del | NP_001131.3:n.*456_*457del | |
NM_001140.5:c.*456_*457del MANE Select | NP_001131.3:n.*456_*457del |