Canonical Allele Identifier:
CA1817441786
Gene:
Linked Data
dbSNP Id:
rs1812775626
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.125478439G>A , CM000670.2:g.125478439G>A | GRCh38 |
| NC_000008.10:g.126490681G>A , CM000670.1:g.126490681G>A | GRCh37 |
| NC_000008.9:g.126559863G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928628.1:n.256+5125G>A |