Canonical Allele Identifier:
CA1702564132
Gene:
Linked Data
dbSNP Id:
rs10441105
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41782358C>T , CM000669.2:g.41782358C>T | GRCh38 |
| NC_000007.13:g.41821956C>T , CM000669.1:g.41821956C>T | GRCh37 |
| NC_000007.12:g.41788481C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745185.1:n.964+46644C>T | ||
| XR_001745186.1:n.954+46654C>T |