Linked Data
MyVariant Identifiers:
chr1:g.186650113G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680981G>A , CM000663.2:g.186680981G>A | GRCh38 |
| NC_000001.10:g.186650113G>A , CM000663.1:g.186650113G>A | GRCh37 |
| NC_000001.9:g.184916736G>A | NCBI36 |
| NG_028206.2:g.4447C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125801.1:n.328G>A |