Linked Data
MyVariant Identifiers:
chr1:g.218518538C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218345196C>T , CM000663.2:g.218345196C>T | GRCh38 |
| NC_000001.10:g.218518538C>T , CM000663.1:g.218518538C>T | GRCh37 |
| NC_000001.9:g.216585161C>T | NCBI36 |
| NG_027721.1:g.4863C>T | |
| NG_027721.2:g.4863C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046268.1:n.269G>A |