Linked Data
MyVariant Identifiers:
chr1:g.186650101G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680969G>A , CM000663.2:g.186680969G>A | GRCh38 |
| NC_000001.10:g.186650101G>A , CM000663.1:g.186650101G>A | GRCh37 |
| NC_000001.9:g.184916724G>A | NCBI36 |
| NG_028206.2:g.4459C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125801.1:n.316G>A |