Canonical Allele Identifier:
CA2037173935
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.53876444C= , CM000674.2:g.53876444C= | GRCh38 |
| NC_000012.11:g.54270228C= , CM000674.1:g.54270228C= | GRCh37 |
| NC_000012.10:g.52556495C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001749153.1:n.375+1196C= | ||
| XR_001749154.1:n.545+1196C= | ||
| XR_002957415.1:n.452-19753C= |