HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740140_67740146del , CM000666.2:g.67740140_67740146del | GRCh38 |
NC_000004.11:g.68605858_68605864del , CM000666.1:g.68605858_68605864del | GRCh37 |
NC_000004.10:g.68288453_68288459del | NCBI36 |
NG_009293.1:g.20941_20947del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.*334_*340del MANE Select | ENSP00000226413.5:n.*334_*340del | |
ENST00000226413.4:c.*334_*340del | ENSP00000226413.4:n.*334_*340del | |
NM_000406.2:c.*334_*340del | NP_000397.1:n.*334_*340del | |
NM_001012763.1:c.*443_*449del | NP_001012781.1:n.*443_*449del | |
NM_000406.3:c.*334_*340del MANE Select | NP_000397.1:n.*334_*340del | |
NM_001012763.2:c.*443_*449del | NP_001012781.1:n.*443_*449del |