Linked Data
gnomAD v4:
3-184059972-C-CG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184059972_184059973insG , CM000665.2:g.184059972_184059973insG | GRCh38 |
| NC_000003.11:g.183777760_183777761insG , CM000665.1:g.183777760_183777761insG | GRCh37 |
| NC_000003.10:g.185260454_185260455insG | NCBI36 |
| NG_012749.1:g.11926_11927insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318351.2:c.1070_1071insG MANE Select | ENSP00000322617.1:p.Gly358ArgfsTer13 | |
| ENST00000318351.1:c.1070_1071insG | ENSP00000322617.1:p.Gly358ArgfsTer13 | |
| NM_130770.2:c.1070_1071insG | NP_570126.2:p.Gly358ArgfsTer13 | |
| NM_130770.3:c.1070_1071insG MANE Select | NP_570126.2:p.Gly358ArgfsTer13 |