Linked Data
dbSNP Id:
rs1873390054
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.72020792_72020793insG , CM000674.2:g.72020792_72020793insG | GRCh38 |
| NC_000012.11:g.72414572_72414573insG , CM000674.1:g.72414572_72414573insG | GRCh37 |
| NC_000012.10:g.70700839_70700840insG | NCBI36 |
| NG_008279.1:g.86947_86948insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333850.4:c.1069-1607_1069-1606insG MANE Select | ENSP00000329093.3:n.1069-1607_1069-1606insG | |
| ENST00000333850.3:c.1069-1607_1069-1606insG | ENSP00000329093.3:n.1069-1607_1069-1606insG | |
| NM_173353.3:c.1069-1607_1069-1606insG | NP_775489.2:n.1069-1607_1069-1606insG | |
| XM_011537899.1:c.475-1607_475-1606insG | XP_011536201.1:n.475-1607_475-1606insG | |
| NM_173353.4:c.1069-1607_1069-1606insG MANE Select | NP_775489.2:n.1069-1607_1069-1606insG |