Linked Data
gnomAD v4:
22-27750780-A-AC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750780_27750781insC , CM000684.2:g.27750780_27750781insC | GRCh38 |
| NC_000022.10:g.28146768_28146769insC , CM000684.1:g.28146768_28146769insC | GRCh37 |
| NC_000022.9:g.26476768_26476769insC | NCBI36 |
| NG_023258.1:g.55718_55719insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.622_623insG | ||
| ENST00000302326.5:c.*134_*135insG MANE Select | ENSP00000304956.4:n.*134_*135insG | |
| ENST00000302326.4:c.*134_*135insG | ENSP00000304956.4:n.*134_*135insG | |
| ENST00000424656.1:c.450_451insG | ||
| ENST00000497225.1:n.453_454insG | ||
| NM_002430.2:c.*134_*135insG | NP_002421.3:n.*134_*135insG | |
| NM_002430.3:c.*134_*135insG MANE Select | NP_002421.3:n.*134_*135insG |