Canonical Allele Identifier:
CA2193710212
Gene:
Linked Data
dbSNP Id:
rs1895000636
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.87419302G>C , CM000677.2:g.87419302G>C | GRCh38 |
| NC_000015.9:g.87962533G>C , CM000677.1:g.87962533G>C | GRCh37 |
| NC_000015.8:g.85763537G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932584.1:n.340-31C>G | ||
| XR_932585.1:n.340-31C>G | ||
| XR_001751647.1:n.617-31C>G | ||
| XR_932585.2:n.627-31C>G |