HGVS | Genome Assembly |
---|---|
NC_000003.12:g.87259848_87259851del , CM000665.2:g.87259848_87259851del | GRCh38 |
NC_000003.11:g.87308998_87309001del , CM000665.1:g.87308998_87309001del | GRCh37 |
NC_000003.10:g.87391688_87391691del | NCBI36 |
NG_008225.2:g.21739_21742del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344265.8:c.*45_*48del | ENSP00000342931.3:n.*45_*48del | |
ENST00000350375.7:c.*45_*48del MANE Select | ENSP00000263781.2:n.*45_*48del | |
ENST00000344265.7:c.*45_*48del | ENSP00000342931.3:n.*45_*48del | |
ENST00000350375.6:c.*45_*48del | ENSP00000263781.2:n.*45_*48del | |
NM_000306.3:c.*45_*48del | NP_000297.1:n.*45_*48del | |
NM_001122757.2:c.*45_*48del | NP_001116229.1:n.*45_*48del | |
NM_000306.4:c.*45_*48del MANE Select | NP_000297.1:n.*45_*48del | |
NM_001122757.3:c.*45_*48del | NP_001116229.1:n.*45_*48del |