Linked Data
dbSNP Id:
rs1555881002
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750781_27750782insT , CM000684.2:g.27750781_27750782insT | GRCh38 |
| NC_000022.10:g.28146769_28146770insT , CM000684.1:g.28146769_28146770insT | GRCh37 |
| NC_000022.9:g.26476769_26476770insT | NCBI36 |
| NG_023258.1:g.55717_55718insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.621_622insA | ||
| ENST00000302326.5:c.*133_*134insA MANE Select | ENSP00000304956.4:n.*133_*134insA | |
| ENST00000302326.4:c.*133_*134insA | ENSP00000304956.4:n.*133_*134insA | |
| ENST00000424656.1:c.449_450insA | ||
| ENST00000497225.1:n.452_453insA | ||
| NM_002430.2:c.*133_*134insA | NP_002421.3:n.*133_*134insA | |
| NM_002430.3:c.*133_*134insA MANE Select | NP_002421.3:n.*133_*134insA |