HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151526652_151526653insCTAGAGGTGTGCACCACCATGC , CM000668.2:g.151526652_151526653insCTAGAGGTGTGCACCACCATGC | GRCh38 |
NC_000006.11:g.151847787_151847788insCTAGAGGTGTGCACCACCATGC , CM000668.1:g.151847787_151847788insCTAGAGGTGTGCACCACCATGC | GRCh37 |
NC_000006.10:g.151889480_151889481insCTAGAGGTGTGCACCACCATGC | NCBI36 |
NG_021198.1:g.37613_37614insCTAGAGGTGTGCACCACCATGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000239374.8:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC MANE Select | ENSP00000239374.6:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC | |
ENST00000239374.7:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC | ENSP00000239374.6:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC | |
NM_025059.3:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC | NP_079335.2:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC | |
NM_025059.4:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC MANE Select | NP_079335.2:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC |