Canonical Allele Identifier:
CA1899263459
Gene:
Linked Data
dbSNP Id:
rs1839589238
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30201664A>G , CM000672.2:g.30201664A>G | GRCh38 |
| NC_000010.10:g.30490593A>G , CM000672.1:g.30490593A>G | GRCh37 |
| NC_000010.9:g.30530599A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930791.1:n.1193-1823A>G | ||
| XR_930791.2:n.1449-1823A>G |