Canonical Allele Identifier:
CA1723810359
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87913747T= , CM000669.2:g.87913747T= | GRCh38 |
| NC_000007.13:g.87543062T= , CM000669.1:g.87543062T= | GRCh37 |
| NC_000007.12:g.87380998T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927723.1:n.148+154A= | ||
| XR_927724.1:n.192+154A= |