Linked Data
dbSNP Id:
rs1756221322
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1414491_1414492insGGGTGGGGGGCCGGGAGGGGCAGGGAAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGG , CM000667.2:g.1414491_1414492insGGGTGGGGGGCCGGGAGGGGCAGGGAAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGG | GRCh38 |
| NC_000005.9:g.1414606_1414607insGGGTGGGGGGCCGGGAGGGGCAGGGAAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGG , CM000667.1:g.1414606_1414607insGGGTGGGGGGCCGGGAGGGGCAGGGAAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGG | GRCh37 |
| NC_000005.8:g.1467606_1467607insGGGTGGGGGGCCGGGAGGGGCAGGGAAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGG | NCBI36 |
| NG_015885.1:g.35937_35938insCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTTCCCTGCCCCTCCCGGCCCCCCACCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTTCCCTGCCCCTCCCGGCCCCCCACCC MANE Select | ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCA... | |
| ENST00000270349.11:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTTCCCTGCCCCTCCCGGCCCCCCACCC | ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCA... | |
| NM_001044.4:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTTCCCTGCCCCTCCCGGCCCCCCACCC | NP_001035.1:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCT... | |
| NM_001044.5:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTTCCCTGCCCCTCCCGGCCCCCCACCC MANE Select | NP_001035.1:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCT... |