Linked Data
gnomAD v4:
20-46016656-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016656T>G , CM000682.2:g.46016656T>G | GRCh38 |
| NC_000020.10:g.44645295T>G , CM000682.1:g.44645295T>G | GRCh37 |
| NC_000020.9:g.44078702T>G | NCBI36 |
| NG_011468.1:g.12749T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_147699.1:n.669-1868A>C |