HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315944_159315945insGC , CM000667.2:g.159315944_159315945insGC | GRCh38 |
NC_000005.9:g.158742952_158742953insGC , CM000667.1:g.158742952_158742953insGC | GRCh37 |
NC_000005.8:g.158675530_158675531insGC | NCBI36 |
NG_009618.1:g.19529_19530insGC , LRG_71:g.19529_19530insGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*156_*157insGC | ENSP00000512849.1:n.*156_*157insGC | |
ENST00000696751.1:c.*638_*639insGC | ENSP00000512850.1:n.*638_*639insGC | |
ENST00000231228.3:c.*156_*157insGC MANE Select | ENSP00000231228.2:n.*156_*157insGC | |
ENST00000231228.2:c.*156_*157insGC | ENSP00000231228.2:n.*156_*157insGC | |
NM_002187.2:c.*156_*157insGC , LRG_71t1:c.*156_*157insGC | NP_002178.2:n.*156_*157insGC | |
NM_002187.3:c.*156_*157insGC MANE Select | NP_002178.2:n.*156_*157insGC |