Canonical Allele Identifier:
CA1139843447
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.205783537A= , CM000663.2:g.205783537A= | GRCh38 |
| NC_000001.10:g.205752665A= , CM000663.1:g.205752665A= | GRCh37 |
| NC_000001.9:g.204019288A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922472.1:n.889A= |