Linked Data
dbSNP Id:
rs1756210249
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1414424_1414425insAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGG , CM000667.2:g.1414424_1414425insAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGG | GRCh38 |
| NC_000005.9:g.1414539_1414540insAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGG , CM000667.1:g.1414539_1414540insAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGG | GRCh37 |
| NC_000005.8:g.1467539_1467540insAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGG | NCBI36 |
| NG_015885.1:g.36004_36005insCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCT MANE Select | ENSP00000270349.9:n.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCC... | |
| ENST00000270349.11:c.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCT | ENSP00000270349.9:n.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCC... | |
| NM_001044.4:c.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCT | NP_001035.1:n.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCCCCCCAC... | |
| NM_001044.5:c.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCT MANE Select | NP_001035.1:n.1156+266_1156+267insCCTGCCCTGACCCTCCCGGCCCCCCAC... |