Canonical Allele Identifier:
CA1563552229
Gene:
Linked Data
dbSNP Id:
rs1744568115
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.92223063A>G , CM000667.2:g.92223063A>G | GRCh38 |
| NC_000005.9:g.91518880A>G , CM000667.1:g.91518880A>G | GRCh37 |
| NC_000005.8:g.91554636A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948565.1:n.394+18379A>G |