Linked Data
dbSNP Id:
rs2102734828
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431395_229431396insTG , CM000663.2:g.229431395_229431396insTG | GRCh38 |
| NC_000001.10:g.229567142_229567143insTG , CM000663.1:g.229567142_229567143insTG | GRCh37 |
| NC_000001.9:g.227633765_227633766insTG | NCBI36 |
| NG_006672.1:g.7701_7702insCA , LRG_429:g.7701_7702insCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.*103_*104insCA | ENSP00000355644.4:n.*103_*104insCA | |
| ENST00000684723.1:c.*103_*104insCA | ENSP00000508084.1:n.*103_*104insCA | |
| ENST00000366683.3:c.*103_*104insCA | ENSP00000355644.3:n.*103_*104insCA | |
| ENST00000366684.7:c.*103_*104insCA MANE Select | ENSP00000355645.3:n.*103_*104insCA | |
| NM_001100.3:c.*103_*104insCA , LRG_429t1:c.*103_*104insCA | NP_001091.1:n.*103_*104insCA | |
| NM_001100.4:c.*103_*104insCA MANE Select | NP_001091.1:n.*103_*104insCA |