Linked Data
dbSNP Id:
rs2108749106
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129528710_129528711insTG , CM000665.2:g.129528710_129528711insTG | GRCh38 |
| NC_000003.11:g.129247553_129247554insTG , CM000665.1:g.129247553_129247554insTG | GRCh37 |
| NC_000003.10:g.130730243_130730244insTG | NCBI36 |
| NG_009115.1:g.5072_5073insTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.-24_-23insTG MANE Select | ENSP00000296271.3:n.-24_-23insTG | |
| ENST00000296271.3:c.-24_-23insTG | ENSP00000296271.3:n.-24_-23insTG | |
| NM_000539.3:c.-24_-23insTG MANE Select | NP_000530.1:n.-24_-23insTG |