Canonical Allele Identifier:
CA1899263488
Gene:
Linked Data
dbSNP Id:
rs1839589780
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30201720C>T , CM000672.2:g.30201720C>T | GRCh38 |
| NC_000010.10:g.30490649C>T , CM000672.1:g.30490649C>T | GRCh37 |
| NC_000010.9:g.30530655C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_930791.1:n.1193-1767C>T | ||
| XR_930791.2:n.1449-1767C>T |