Linked Data
gnomAD v4:
20-46016568-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016568G>T , CM000682.2:g.46016568G>T | GRCh38 |
| NC_000020.10:g.44645207G>T , CM000682.1:g.44645207G>T | GRCh37 |
| NC_000020.9:g.44078614G>T | NCBI36 |
| NG_011468.1:g.12661G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_147699.1:n.669-1780C>A |