Canonical Allele Identifier:
CA2263926949
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50211769G= , CM000679.2:g.50211769G= | GRCh38 |
| NC_000017.10:g.48289130G= , CM000679.1:g.48289130G= | GRCh37 |
| NC_000017.9:g.45644129G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934838.1:n.43-2066G= |