Canonical Allele Identifier:
CA2580760889
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87913722C>T , CM000669.2:g.87913722C>T | GRCh38 |
| NC_000007.13:g.87543037C>T , CM000669.1:g.87543037C>T | GRCh37 |
| NC_000007.12:g.87380973C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927723.1:n.148+179G>A | ||
| XR_927724.1:n.192+179G>A |