HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190408_204190409insGGGG , CM000663.2:g.204190408_204190409insGGGG | GRCh38 |
NC_000001.10:g.204159536_204159537insGGGG , CM000663.1:g.204159536_204159537insGGGG | GRCh37 |
NC_000001.9:g.202426159_202426160insGGGG | NCBI36 |
NG_032151.1:g.11084_11085insCCCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*76_*77insCCCC MANE Select | ENSP00000356162.4:n.*76_*77insCCCC | |
ENST00000367194.4:c.*76_*77insCCCC | ENSP00000356162.4:n.*76_*77insCCCC | |
NM_002256.3:c.*76_*77insCCCC | NP_002247.3:n.*76_*77insCCCC | |
XM_011509525.1:c.*76_*77insCCCC | XP_011507827.1:n.*76_*77insCCCC | |
NM_002256.4:c.*76_*77insCCCC MANE Select | NP_002247.3:n.*76_*77insCCCC |