Linked Data
dbSNP Id:
rs1756212087
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1414459_1414460insAGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCGGGAGGGGCAGGGC , CM000667.2:g.1414459_1414460insAGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCGGGAGGGGCAGGGC | GRCh38 |
| NC_000005.9:g.1414574_1414575insAGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCGGGAGGGGCAGGGC , CM000667.1:g.1414574_1414575insAGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCGGGAGGGGCAGGGC | GRCh37 |
| NC_000005.8:g.1467574_1467575insAGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCGCTGGGTGGGGGGCCGGGAGGGGCAGGGC | NCBI36 |
| NG_015885.1:g.35997_35998insCGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCTGCCCTGCCCCTCCCGGCCCCCCACCCAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCTGCCCTGCCCCTCCCGGCCCCCCACCCAG MANE Select | ENSP00000270349.9:n.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCT... | |
| ENST00000270349.11:c.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCTGCCCTGCCCCTCCCGGCCCCCCACCCAG | ENSP00000270349.9:n.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCT... | |
| NM_001044.4:c.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCTGCCCTGCCCCTCCCGGCCCCCCACCCAG | NP_001035.1:n.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCTCCAGGC... | |
| NM_001044.5:c.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCTGCCCTGCCCCTCCCGGCCCCCCACCCAG MANE Select | NP_001035.1:n.1156+259_1156+260insCGCCTTCCCCGCCCTGCCCCTCCAGGC... |