Linked Data
MyVariant Identifiers:
chr1:g.186650478A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186681346A>G , CM000663.2:g.186681346A>G | GRCh38 |
| NC_000001.10:g.186650478A>G , CM000663.1:g.186650478A>G | GRCh37 |
| NC_000001.9:g.184917101A>G | NCBI36 |
| NG_028206.2:g.4082T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125801.1:n.693A>G |