Canonical Allele Identifier:
CA1968513089
Gene:
Linked Data
dbSNP Id:
rs1856778874
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.45506633G>A , CM000673.2:g.45506633G>A | GRCh38 |
| NC_000011.9:g.45528183G>A , CM000673.1:g.45528183G>A | GRCh37 |
| NC_000011.8:g.45484759G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001748204.2:n.909-16862C>T | ||
| XR_931245.3:n.566-16862C>T |