Linked Data
MyVariant Identifiers:
chr20:g.58895744A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.60320686A>C , CM000682.2:g.60320686A>C | GRCh38 |
| NC_000020.10:g.58895744A>C , CM000682.1:g.58895744A>C | GRCh37 |
| NC_000020.9:g.58329139A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046099.1:n.473A>C |