Canonical Allele Identifier:
CA2129379013
Gene:
Linked Data
dbSNP Id:
rs1882059445
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36384757C>G , CM000676.2:g.36384757C>G | GRCh38 |
| NC_000014.8:g.36853962C>G , CM000676.1:g.36853962C>G | GRCh37 |
| NC_000014.7:g.35923713C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537428.1:c.319-12402C>G | XP_011535730.1:n.319-12402C>G | |
| XR_943756.1:n.358+23661C>G |