Canonical Allele Identifier:
CA1841175533
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551361T>C , CM000671.2:g.25551361T>C | GRCh38 |
| NC_000009.11:g.25551359T>C , CM000671.1:g.25551359T>C | GRCh37 |
| NC_000009.10:g.25541359T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-789A>G | ||
| XR_929525.2:n.674-789A>G |