Canonical Allele Identifier:
CA2263926892
Gene:
Linked Data
dbSNP Id:
rs1908567299
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50211652G>A , CM000679.2:g.50211652G>A | GRCh38 |
| NC_000017.10:g.48289013G>A , CM000679.1:g.48289013G>A | GRCh37 |
| NC_000017.9:g.45644012G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934838.1:n.43-2183G>A |