Canonical Allele Identifier:
CA1161925222
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34523581C= , CM000663.2:g.34523581C= | GRCh38 |
| NC_000001.10:g.34989182C= , CM000663.1:g.34989182C= | GRCh37 |
| NC_000001.9:g.34761769C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947171.1:n.1073+23998G= | ||
| XR_001737964.1:n.991+23998G= |