Linked Data
gnomAD v4:
17-41584058-T-TCG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584059_41584060insGC , CM000679.2:g.41584059_41584060insGC | GRCh38 |
| NC_000017.10:g.39740311_39740312insGC , CM000679.1:g.39740311_39740312insGC | GRCh37 |
| NC_000017.9:g.36993837_36993838insGC | NCBI36 |
| NG_008624.1:g.7837_7838insCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-138_766-137insCG MANE Select | ENSP00000167586.6:n.766-138_766-137insCG | |
| ENST00000167586.6:c.766-138_766-137insCG | ENSP00000167586.6:n.766-138_766-137insCG | |
| ENST00000476662.1:n.216-138_216-137insCG | ||
| NM_000526.4:c.766-138_766-137insCG | NP_000517.2:n.766-138_766-137insCG | |
| NM_000526.5:c.766-138_766-137insCG MANE Select | NP_000517.3:n.766-138_766-137insCG |