Linked Data
gnomAD v4:
4-186191799-C-CG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186191799_186191800insG , CM000666.2:g.186191799_186191800insG | GRCh38 |
| NC_000004.11:g.187112953_187112954insG , CM000666.1:g.187112953_187112954insG | GRCh37 |
| NC_000004.10:g.187349947_187349948insG | NCBI36 |
| NG_007965.1:g.5280_5281insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.-25_-24insG MANE Select | ENSP00000368079.4:n.-25_-24insG | |
| ENST00000378802.4:c.-25_-24insG | ENSP00000368079.4:n.-25_-24insG | |
| NM_207352.3:c.-25_-24insG | NP_997235.3:n.-25_-24insG | |
| XM_005262935.2:c.-25_-24insG | XP_005262992.1:n.-25_-24insG | |
| XM_005262935.4:c.-25_-24insG | XP_005262992.1:n.-25_-24insG | |
| XM_017008037.1:c.-335_-334insG | XP_016863526.1:n.-335_-334insG | |
| NM_207352.4:c.-25_-24insG MANE Select | NP_997235.3:n.-25_-24insG |