Canonical Allele Identifier:
CA2332763258
Gene:
Linked Data
dbSNP Id:
rs962348533
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521951C>G , CM000681.2:g.33521951C>G | GRCh38 |
| NC_000019.9:g.34012857C>G , CM000681.1:g.34012857C>G | GRCh37 |
| NC_000019.8:g.38704697C>G | NCBI36 |
| NG_013358.1:g.4943G>C | |
| NG_013358.2:g.4943G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.10C>G | ||
| XR_935919.1:n.5C>G | ||
| XR_001754035.2:n.18C>G | ||
| XR_935918.2:n.18C>G |