Canonical Allele Identifier:
CA2197670097
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.95613139A= , CM000677.2:g.95613139A= | GRCh38 |
| NC_000015.9:g.96156368A= , CM000677.1:g.96156368A= | GRCh37 |
| NC_000015.8:g.93957372A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932654.1:n.68+3063A= |