Linked Data
MyVariant Identifiers:
chr20:g.58895775C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.60320717C>A , CM000682.2:g.60320717C>A | GRCh38 |
| NC_000020.10:g.58895775C>A , CM000682.1:g.58895775C>A | GRCh37 |
| NC_000020.9:g.58329170C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046099.1:n.504C>A |