Linked Data
gnomAD v4:
20-46016616-C-CCTG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016616_46016617insCTG , CM000682.2:g.46016616_46016617insCTG | GRCh38 |
| NC_000020.10:g.44645255_44645256insCTG , CM000682.1:g.44645255_44645256insCTG | GRCh37 |
| NC_000020.9:g.44078662_44078663insCTG | NCBI36 |
| NG_011468.1:g.12709_12710insCTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_147699.1:n.669-1829_669-1828insCAG |