Canonical Allele Identifier:
CA1205766069
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649561A= , CM000663.2:g.168649561A= | GRCh38 |
| NC_000001.10:g.168618799A= , CM000663.1:g.168618799A= | GRCh37 |
| NC_000001.9:g.166885423A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-8286T= | ||
| XR_922259.2:n.332-8286T= |