Linked Data
MyVariant Identifiers:
chr1:g.186650559A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186681427A>C , CM000663.2:g.186681427A>C | GRCh38 |
| NC_000001.10:g.186650559A>C , CM000663.1:g.186650559A>C | GRCh37 |
| NC_000001.9:g.184917182A>C | NCBI36 |
| NG_028206.2:g.4001T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125801.1:n.774A>C |