HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315925_159315926insCC , CM000667.2:g.159315925_159315926insCC | GRCh38 |
NC_000005.9:g.158742933_158742934insCC , CM000667.1:g.158742933_158742934insCC | GRCh37 |
NC_000005.8:g.158675511_158675512insCC | NCBI36 |
NG_009618.1:g.19548_19549insGG , LRG_71:g.19548_19549insGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*175_*176insGG | ENSP00000512849.1:n.*175_*176insGG | |
ENST00000696751.1:c.*657_*658insGG | ENSP00000512850.1:n.*657_*658insGG | |
ENST00000231228.3:c.*175_*176insGG MANE Select | ENSP00000231228.2:n.*175_*176insGG | |
ENST00000231228.2:c.*175_*176insGG | ENSP00000231228.2:n.*175_*176insGG | |
NM_002187.2:c.*175_*176insGG , LRG_71t1:c.*175_*176insGG | NP_002178.2:n.*175_*176insGG | |
NM_002187.3:c.*175_*176insGG MANE Select | NP_002178.2:n.*175_*176insGG |