HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461608_122461609delinsGC , CM000672.2:g.122461608_122461609delinsGC | GRCh38 |
NC_000010.10:g.124221124_124221125delinsGC , CM000672.1:g.124221124_124221125delinsGC | GRCh37 |
NC_000010.9:g.124211114_124211115delinsGC | NCBI36 |
NG_011554.1:g.5084_5085delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.-45_-44delinsGC MANE Select | ENSP00000357980.3:n.-45_-44delinsGC | |
ENST00000648167.1:c.154+2899_154+2900delinsGC | ENSP00000498033.1:n.154+2899_154+2900delinsGC | |
ENST00000368984.7:c.-45_-44delinsGC | ENSP00000357980.3:n.-45_-44delinsGC | |
NM_002775.4:c.-45_-44delinsGC | NP_002766.1:n.-45_-44delinsGC | |
NM_002775.5:c.-45_-44delinsGC MANE Select | NP_002766.1:n.-45_-44delinsGC |