Canonical Allele Identifier:
CA1161925252
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34523647A= , CM000663.2:g.34523647A= | GRCh38 |
| NC_000001.10:g.34989248A= , CM000663.1:g.34989248A= | GRCh37 |
| NC_000001.9:g.34761835A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_947171.1:n.1073+23932T= | ||
| XR_001737964.1:n.991+23932T= |