Canonical Allele Identifier:
CA2263926879
Gene:
Linked Data
dbSNP Id:
rs1908566748
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50211614C>G , CM000679.2:g.50211614C>G | GRCh38 |
| NC_000017.10:g.48288975C>G , CM000679.1:g.48288975C>G | GRCh37 |
| NC_000017.9:g.45643974C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934838.1:n.42+2208C>G |