HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713997_114713998insCC , CM000663.2:g.114713997_114713998insCC | GRCh38 |
NC_000001.10:g.115256618_115256619insCC , CM000663.1:g.115256618_115256619insCC | GRCh37 |
NC_000001.9:g.115058141_115058142insCC | NCBI36 |
NG_007572.1:g.7897_7898insGG , LRG_92:g.7897_7898insGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-20_112-19insGG MANE Select | ENSP00000358548.4:n.112-20_112-19insGG | |
ENST00000369535.4:c.112-20_112-19insGG | ENSP00000358548.4:n.112-20_112-19insGG | |
NM_002524.4:c.112-20_112-19insGG | NP_002515.1:n.112-20_112-19insGG | |
NM_002524.5:c.112-20_112-19insGG MANE Select | NP_002515.1:n.112-20_112-19insGG |