Linked Data
dbSNP Id:
rs2102734939
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431484_229431485insTCG , CM000663.2:g.229431484_229431485insTCG | GRCh38 |
| NC_000001.10:g.229567231_229567232insTCG , CM000663.1:g.229567231_229567232insTCG | GRCh37 |
| NC_000001.9:g.227633854_227633855insTCG | NCBI36 |
| NG_006672.1:g.7613_7614insGAC , LRG_429:g.7613_7614insGAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.*15_*16insGAC | ENSP00000355644.4:n.*15_*16insGAC | |
| ENST00000684723.1:c.*15_*16insGAC | ENSP00000508084.1:n.*15_*16insGAC | |
| ENST00000366683.3:c.*15_*16insGAC | ENSP00000355644.3:n.*15_*16insGAC | |
| ENST00000366684.7:c.*15_*16insGAC MANE Select | ENSP00000355645.3:n.*15_*16insGAC | |
| NM_001100.3:c.*15_*16insGAC , LRG_429t1:c.*15_*16insGAC | NP_001091.1:n.*15_*16insGAC | |
| NM_001100.4:c.*15_*16insGAC MANE Select | NP_001091.1:n.*15_*16insGAC |