Canonical Allele Identifier:
CA2298481247
Gene:
Linked Data
dbSNP Id:
rs1910118770
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.41477691C>T , CM000680.2:g.41477691C>T | GRCh38 |
| NC_000018.9:g.39057655C>T , CM000680.1:g.39057655C>T | GRCh37 |
| NC_000018.8:g.37311653C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935409.1:n.86-26443C>T |