HGVS | Genome Assembly |
---|---|
NC_000012.12:g.72020870_72020871delinsTG , CM000674.2:g.72020870_72020871delinsTG | GRCh38 |
NC_000012.11:g.72414650_72414651delinsTG , CM000674.1:g.72414650_72414651delinsTG | GRCh37 |
NC_000012.10:g.70700917_70700918delinsTG | NCBI36 |
NG_008279.1:g.87025_87026delinsTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000333850.4:c.1069-1529_1069-1528delinsTG MANE Select | ENSP00000329093.3:n.1069-1529_1069-1528de... | |
ENST00000333850.3:c.1069-1529_1069-1528delinsTG | ENSP00000329093.3:n.1069-1529_1069-1528de... | |
NM_173353.3:c.1069-1529_1069-1528delinsTG | NP_775489.2:n.1069-1529_1069-1528delinsTG... | |
XM_011537899.1:c.475-1529_475-1528delinsTG | XP_011536201.1:n.475-1529_475-1528delinsT... | |
NM_173353.4:c.1069-1529_1069-1528delinsTG MANE Select | NP_775489.2:n.1069-1529_1069-1528delinsTG... |