Canonical Allele Identifier:
CA1140138322
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.220491610G= , CM000663.2:g.220491610G= | GRCh38 |
| NC_000001.10:g.220664952G= , CM000663.1:g.220664952G= | GRCh37 |
| NC_000001.9:g.218731575G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922615.1:n.256-624G= | ||
| XR_001737822.1:n.557-624G= |