Linked Data
MyVariant Identifiers:
chr20:g.58895867C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.60320809C>T , CM000682.2:g.60320809C>T | GRCh38 |
| NC_000020.10:g.58895867C>T , CM000682.1:g.58895867C>T | GRCh37 |
| NC_000020.9:g.58329262C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046099.1:n.596C>T |