Canonical Allele Identifier:
CA1740470142
Gene:
Linked Data
dbSNP Id:
rs1795646735
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.124306389C>G , CM000669.2:g.124306389C>G | GRCh38 |
| NC_000007.13:g.123946443C>G , CM000669.1:g.123946443C>G | GRCh37 |
| NC_000007.12:g.123733679C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_002956584.1:n.73-89C>G |