Canonical Allele Identifier:
CA1605276929
Gene:
Linked Data
dbSNP Id:
rs1581256759
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.466005T>G , CM000668.2:g.466005T>G | GRCh38 |
| NC_000006.11:g.466005T>G , CM000668.1:g.466005T>G | GRCh37 |
| NC_000006.10:g.411005T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926364.1:n.2714+12280T>G | ||
| XR_926365.1:n.2548+12280T>G | ||
| XR_001743914.1:n.482-9203T>G |