HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884713_149884714insGCC , CM000663.2:g.149884713_149884714insGCC | GRCh38 |
NC_000001.10:g.149856263_149856264insGCC , CM000663.1:g.149856263_149856264insGCC | GRCh37 |
NC_000001.9:g.148122887_148122888insGCC | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369155.4:c.*1546_*1547insGGC MANE Select | ENSP00000358151.2:n.*1546_*1547insGGC | |
ENST00000369155.3:c.*1546_*1547insGGC | ENSP00000358151.2:n.*1546_*1547insGGC | |
ENST00000369160.3:c.377+1550_377+1551insGGC | ENSP00000375736.2:n.377+1550_377+1551insG... | |
NM_003528.2:c.*1546_*1547insGGC | NP_003519.1:n.*1546_*1547insGGC | |
NM_003528.3:c.*1546_*1547insGGC MANE Select | NP_003519.1:n.*1546_*1547insGGC |