Linked Data
gnomAD v4:
17-41584060-T-TCC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584061_41584062insCC , CM000679.2:g.41584061_41584062insCC | GRCh38 |
| NC_000017.10:g.39740313_39740314insCC , CM000679.1:g.39740313_39740314insCC | GRCh37 |
| NC_000017.9:g.36993839_36993840insCC | NCBI36 |
| NG_008624.1:g.7835_7836insGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-140_766-139insGG MANE Select | ENSP00000167586.6:n.766-140_766-139insGG | |
| ENST00000167586.6:c.766-140_766-139insGG | ENSP00000167586.6:n.766-140_766-139insGG | |
| ENST00000476662.1:n.216-140_216-139insGG | ||
| NM_000526.4:c.766-140_766-139insGG | NP_000517.2:n.766-140_766-139insGG | |
| NM_000526.5:c.766-140_766-139insGG MANE Select | NP_000517.3:n.766-140_766-139insGG |