Linked Data
MyVariant Identifiers:
chr1:g.218518545T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218345203T>C , CM000663.2:g.218345203T>C | GRCh38 |
| NC_000001.10:g.218518545T>C , CM000663.1:g.218518545T>C | GRCh37 |
| NC_000001.9:g.216585168T>C | NCBI36 |
| NG_027721.1:g.4870T>C | |
| NG_027721.2:g.4870T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046268.1:n.262A>G |