Canonical Allele Identifier:
CA1605276793
Gene:
Linked Data
dbSNP Id:
rs1762567046
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.465805G>C , CM000668.2:g.465805G>C | GRCh38 |
| NC_000006.11:g.465805G>C , CM000668.1:g.465805G>C | GRCh37 |
| NC_000006.10:g.410805G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926364.1:n.2714+12080G>C | ||
| XR_926365.1:n.2548+12080G>C | ||
| XR_001743914.1:n.482-9403G>C |