HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190409_204190410insTGTCCCCCCCCCCCC , CM000663.2:g.204190409_204190410insTGTCCCCCCCCCCCC | GRCh38 |
NC_000001.10:g.204159537_204159538insTGTCCCCCCCCCCCC , CM000663.1:g.204159537_204159538insTGTCCCCCCCCCCCC | GRCh37 |
NC_000001.9:g.202426160_202426161insTGTCCCCCCCCCCCC | NCBI36 |
NG_032151.1:g.11082_11083insGGGGGGGGGGGGACA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*74_*75insGGGGGGGGGGGGACA MANE Select | ENSP00000356162.4:n.*74_*75insGGGGGGGGGGGGACA | |
ENST00000367194.4:c.*74_*75insGGGGGGGGGGGGACA | ENSP00000356162.4:n.*74_*75insGGGGGGGGGGGGACA | |
NM_002256.3:c.*74_*75insGGGGGGGGGGGGACA | NP_002247.3:n.*74_*75insGGGGGGGGGGGGACA | |
XM_011509525.1:c.*74_*75insGGGGGGGGGGGGACA | XP_011507827.1:n.*74_*75insGGGGGGGGGGGGACA | |
NM_002256.4:c.*74_*75insGGGGGGGGGGGGACA MANE Select | NP_002247.3:n.*74_*75insGGGGGGGGGGGGACA |