Linked Data
gnomAD v4:
17-41584064-T-TCG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584065_41584066insGC , CM000679.2:g.41584065_41584066insGC | GRCh38 |
| NC_000017.10:g.39740317_39740318insGC , CM000679.1:g.39740317_39740318insGC | GRCh37 |
| NC_000017.9:g.36993843_36993844insGC | NCBI36 |
| NG_008624.1:g.7831_7832insCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-144_766-143insCG MANE Select | ENSP00000167586.6:n.766-144_766-143insCG | |
| ENST00000167586.6:c.766-144_766-143insCG | ENSP00000167586.6:n.766-144_766-143insCG | |
| ENST00000476662.1:n.216-144_216-143insCG | ||
| NM_000526.4:c.766-144_766-143insCG | NP_000517.2:n.766-144_766-143insCG | |
| NM_000526.5:c.766-144_766-143insCG MANE Select | NP_000517.3:n.766-144_766-143insCG |