Linked Data
MyVariant Identifiers:
chr1:g.218518553T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218345211T>C , CM000663.2:g.218345211T>C | GRCh38 |
| NC_000001.10:g.218518553T>C , CM000663.1:g.218518553T>C | GRCh37 |
| NC_000001.9:g.216585176T>C | NCBI36 |
| NG_027721.1:g.4878T>C | |
| NG_027721.2:g.4878T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046268.1:n.254A>G |