Canonical Allele Identifier:
CA1901528889
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.35006503C>T , CM000672.2:g.35006503C>T | GRCh38 |
| NC_000010.10:g.35295431C>T , CM000672.1:g.35295431C>T | GRCh37 |
| NC_000010.9:g.35335437C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930817.1:n.350-250G>A |