Canonical Allele Identifier:
CA2838210173
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.29650274C>T , CM000663.2:g.29650274C>T | GRCh38 |
| NC_000001.10:g.30123121C>T , CM000663.1:g.30123121C>T | GRCh37 |
| NC_000001.9:g.29895708C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001737956.1:n.221-28845C>T | ||
| XR_001737957.1:n.221-28845C>T | ||
| XR_001737958.1:n.221-28845C>T |