Canonical Allele Identifier:
CA1649534202
Gene:
Linked Data
dbSNP Id:
rs1773158421
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98102339A>G , CM000668.2:g.98102339A>G | GRCh38 |
| NC_000006.11:g.98550215A>G , CM000668.1:g.98550215A>G | GRCh37 |
| NC_000006.10:g.98656936A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245563.2:n.456+3069A>G | ||
| XR_942809.1:n.456+3069A>G |