Canonical Allele Identifier:
CA2193585478
Gene:
Linked Data
dbSNP Id:
rs2082249238
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.87152219C>A , CM000677.2:g.87152219C>A | GRCh38 |
| NC_000015.9:g.87695450C>A , CM000677.1:g.87695450C>A | GRCh37 |
| NC_000015.8:g.85496454C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932582.1:n.167-26008C>A | ||
| XR_932582.2:n.167-26008C>A |