Canonical Allele Identifier:
CA1723810368
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87913767C= , CM000669.2:g.87913767C= | GRCh38 |
| NC_000007.13:g.87543082C= , CM000669.1:g.87543082C= | GRCh37 |
| NC_000007.12:g.87381018C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927723.1:n.148+134G= | ||
| XR_927724.1:n.192+134G= |