HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151526655_151526656insGAGGTGTGCACCACCATGC , CM000668.2:g.151526655_151526656insGAGGTGTGCACCACCATGC | GRCh38 |
NC_000006.11:g.151847790_151847791insGAGGTGTGCACCACCATGC , CM000668.1:g.151847790_151847791insGAGGTGTGCACCACCATGC | GRCh37 |
NC_000006.10:g.151889483_151889484insGAGGTGTGCACCACCATGC | NCBI36 |
NG_021198.1:g.37616_37617insGAGGTGTGCACCACCATGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000239374.8:c.58-9663_58-9662insGAGGTGTGCACCACCATGC MANE Select | ENSP00000239374.6:n.58-9663_58-9662insGAGGTGTGCACCACCATGC | |
ENST00000239374.7:c.58-9663_58-9662insGAGGTGTGCACCACCATGC | ENSP00000239374.6:n.58-9663_58-9662insGAGGTGTGCACCACCATGC | |
NM_025059.3:c.58-9663_58-9662insGAGGTGTGCACCACCATGC | NP_079335.2:n.58-9663_58-9662insGAGGTGTGCACCACCATGC | |
NM_025059.4:c.58-9663_58-9662insGAGGTGTGCACCACCATGC MANE Select | NP_079335.2:n.58-9663_58-9662insGAGGTGTGCACCACCATGC |