Canonical Allele Identifier:
CA2581535169
Community Standard Title: NC_000006.12:g.466033C>G
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.466033C>G , CM000668.2:g.466033C>G | GRCh38 |
| NC_000006.11:g.466033C>G , CM000668.1:g.466033C>G | GRCh37 |
| NC_000006.10:g.411033C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001743914.1:n.482-9175C>G | |
| XR_926364.1:n.2714+12308C>G | |
| XR_926365.1:n.2548+12308C>G |