Linked Data
dbSNP Id:
rs1712788183
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.150926290_150926291insC , CM000665.2:g.150926290_150926291insC | GRCh38 |
| NC_000003.11:g.150644077_150644078insC , CM000665.1:g.150644077_150644078insC | GRCh37 |
| NC_000003.10:g.152126767_152126768insC | NCBI36 |
| NG_009168.1:g.51709_51710insG , LRG_700:g.51709_51710insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295911.6:c.*561_*562insG | ENSP00000295911.2:n.*561_*562insG | |
| ENST00000562308.5:c.104+15291_104+15292insG | ||
| ENST00000565169.1:c.162+15291_162+15292insG | ||
| ENST00000569170.5:c.162+15291_162+15292insG | ||
| NM_052995.2:c.*561_*562insG , LRG_700t2:c.*561_*562insG | NP_443721.1:n.*561_*562insG | |
| XR_924167.1:n.2656_2657insG |