Linked Data
dbSNP Id:
rs1756205973
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1414404_1414405insCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGG , CM000667.2:g.1414404_1414405insCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGG | GRCh38 |
| NC_000005.9:g.1414519_1414520insCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGG , CM000667.1:g.1414519_1414520insCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGG | GRCh37 |
| NC_000005.8:g.1467519_1467520insCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGG | NCBI36 |
| NG_015885.1:g.36029_36030insACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCC MANE Select | ENSP00000270349.9:n.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCT... | |
| ENST00000270349.11:c.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCC | ENSP00000270349.9:n.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCT... | |
| NM_001044.4:c.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCC | NP_001035.1:n.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCTGCCCCT... | |
| NM_001044.5:c.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCC MANE Select | NP_001035.1:n.1156+291_1156+292insACCCAGTGCCTTCTCCGCCCTGCCCCT... |