Canonical Allele Identifier:
CA565006069
Community Standard Title: NC_000006.12:g.466033C>A
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.466033C>A , CM000668.2:g.466033C>A | GRCh38 |
| NC_000006.11:g.466033C>A , CM000668.1:g.466033C>A | GRCh37 |
| NC_000006.10:g.411033C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001743914.1:n.482-9175C>A | |
| XR_926364.1:n.2714+12308C>A | |
| XR_926365.1:n.2548+12308C>A |