Linked Data
gnomAD v4:
21-45990490-A-AGGGATGGG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990491_45990492insGGATGGGG , CM000683.2:g.45990491_45990492insGGATGGGG | GRCh38 |
| NC_000021.8:g.47410405_47410406insGGATGGGG , CM000683.1:g.47410405_47410406insGGATGGGG | GRCh37 |
| NC_000021.7:g.46234833_46234834insGGATGGGG | NCBI36 |
| NG_008674.1:g.13743_13744insGGATGGGG , LRG_475:g.13743_13744insGGATGGGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1002+69_1002+70insGGATGGGG MANE Select | ENSP00000355180.3:n.1002+69_1002+70insGGATGGGG | |
| ENST00000361866.7:c.1002+69_1002+70insGGATGGGG | ENSP00000355180.3:n.1002+69_1002+70insGGATGGGG | |
| ENST00000612273.1:c.1002+69_1002+70insGGATGGGG | ENSP00000483630.1:n.1002+69_1002+70insGGATGGGG | |
| NM_001848.2:c.1002+69_1002+70insGGATGGGG , LRG_475t1:c.1002+69_1002+70insGGATGGGG | NP_001839.2:n.1002+69_1002+70insGGATGGGG | |
| NM_001848.3:c.1002+69_1002+70insGGATGGGG MANE Select | NP_001839.2:n.1002+69_1002+70insGGATGGGG |