Linked Data
MyVariant Identifiers:
chr18:g.56116832A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.58449600A>C , CM000680.2:g.58449600A>C | GRCh38 |
| NC_000018.9:g.56116832A>C , CM000680.1:g.56116832A>C | GRCh37 |
| NC_000018.8:g.54267812A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001753465.2:n.839A>C | ||
| NR_170243.1:n.307+60A>C | ||
| NR_170244.1:n.307+60A>C | ||
| NR_170245.1:n.307+60A>C |