HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190420_204190421insCCCCCCCC , CM000663.2:g.204190420_204190421insCCCCCCCC | GRCh38 |
NC_000001.10:g.204159548_204159549insCCCCCCCC , CM000663.1:g.204159548_204159549insCCCCCCCC | GRCh37 |
NC_000001.9:g.202426171_202426172insCCCCCCCC | NCBI36 |
NG_032151.1:g.11077_11078insGGGGGGGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*69_*70insGGGGGGGG MANE Select | ENSP00000356162.4:n.*69_*70insGGGGGGGG | |
ENST00000367194.4:c.*69_*70insGGGGGGGG | ENSP00000356162.4:n.*69_*70insGGGGGGGG | |
NM_002256.3:c.*69_*70insGGGGGGGG | NP_002247.3:n.*69_*70insGGGGGGGG | |
XM_011509525.1:c.*69_*70insGGGGGGGG | XP_011507827.1:n.*69_*70insGGGGGGGG | |
NM_002256.4:c.*69_*70insGGGGGGGG MANE Select | NP_002247.3:n.*69_*70insGGGGGGGG |