Canonical Allele Identifier:
CA1702564134
Gene:
Linked Data
dbSNP Id:
rs1309963849
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41782371A>G , CM000669.2:g.41782371A>G | GRCh38 |
| NC_000007.13:g.41821969A>G , CM000669.1:g.41821969A>G | GRCh37 |
| NC_000007.12:g.41788494A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745185.1:n.964+46657A>G | ||
| XR_001745186.1:n.954+46667A>G |