Linked Data
MyVariant Identifiers:
chr1:g.218518594C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218345252C>G , CM000663.2:g.218345252C>G | GRCh38 |
| NC_000001.10:g.218518594C>G , CM000663.1:g.218518594C>G | GRCh37 |
| NC_000001.9:g.216585217C>G | NCBI36 |
| NG_027721.1:g.4919C>G | |
| NG_027721.2:g.4919C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046268.1:n.213G>C |