Canonical Allele Identifier:
CA2197752699
Gene:
Linked Data
dbSNP Id:
rs1899530901
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.95782380C>G , CM000677.2:g.95782380C>G | GRCh38 |
| NC_000015.9:g.96325609C>G , CM000677.1:g.96325609C>G | GRCh37 |
| NC_000015.8:g.94126613C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932654.1:n.148-42809C>G |