HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190409_204190410insTCCCCCCCCCCCC , CM000663.2:g.204190409_204190410insTCCCCCCCCCCCC | GRCh38 |
NC_000001.10:g.204159537_204159538insTCCCCCCCCCCCC , CM000663.1:g.204159537_204159538insTCCCCCCCCCCCC | GRCh37 |
NC_000001.9:g.202426160_202426161insTCCCCCCCCCCCC | NCBI36 |
NG_032151.1:g.11082_11083insGGGGGGGGGGGGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*74_*75insGGGGGGGGGGGGA MANE Select | ENSP00000356162.4:n.*74_*75insGGGGGGGGGGGGA | |
ENST00000367194.4:c.*74_*75insGGGGGGGGGGGGA | ENSP00000356162.4:n.*74_*75insGGGGGGGGGGGGA | |
NM_002256.3:c.*74_*75insGGGGGGGGGGGGA | NP_002247.3:n.*74_*75insGGGGGGGGGGGGA | |
XM_011509525.1:c.*74_*75insGGGGGGGGGGGGA | XP_011507827.1:n.*74_*75insGGGGGGGGGGGGA | |
NM_002256.4:c.*74_*75insGGGGGGGGGGGGA MANE Select | NP_002247.3:n.*74_*75insGGGGGGGGGGGGA |