HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315934_159315935insAC , CM000667.2:g.159315934_159315935insAC | GRCh38 |
NC_000005.9:g.158742942_158742943insAC , CM000667.1:g.158742942_158742943insAC | GRCh37 |
NC_000005.8:g.158675520_158675521insAC | NCBI36 |
NG_009618.1:g.19539_19540insGT , LRG_71:g.19539_19540insGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*166_*167insGT | ENSP00000512849.1:n.*166_*167insGT | |
ENST00000696751.1:c.*648_*649insGT | ENSP00000512850.1:n.*648_*649insGT | |
ENST00000231228.3:c.*166_*167insGT MANE Select | ENSP00000231228.2:n.*166_*167insGT | |
ENST00000231228.2:c.*166_*167insGT | ENSP00000231228.2:n.*166_*167insGT | |
NM_002187.2:c.*166_*167insGT , LRG_71t1:c.*166_*167insGT | NP_002178.2:n.*166_*167insGT | |
NM_002187.3:c.*166_*167insGT MANE Select | NP_002178.2:n.*166_*167insGT |