Canonical Allele Identifier:
CA2263927011
Gene:
Linked Data
dbSNP Id:
rs1567770262
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50211906G>A , CM000679.2:g.50211906G>A | GRCh38 |
| NC_000017.10:g.48289267G>A , CM000679.1:g.48289267G>A | GRCh37 |
| NC_000017.9:g.45644266G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934838.1:n.43-1929G>A |