Canonical Allele Identifier:
CA1605276836
Gene:
Linked Data
dbSNP Id:
rs965732289
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.465876C>A , CM000668.2:g.465876C>A | GRCh38 |
| NC_000006.11:g.465876C>A , CM000668.1:g.465876C>A | GRCh37 |
| NC_000006.10:g.410876C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926364.1:n.2714+12151C>A | ||
| XR_926365.1:n.2548+12151C>A | ||
| XR_001743914.1:n.482-9332C>A |