Canonical Allele Identifier:
CA2568848617
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.123753556C>T , CM000670.2:g.123753556C>T | GRCh38 |
| NC_000008.10:g.124765796C>T , CM000670.1:g.124765796C>T | GRCh37 |
| NC_000008.9:g.124834977C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928607.1:n.153-11227C>T | ||
| XR_928607.3:n.324-11227C>T |