Canonical Allele Identifier:
CA1841175569
Gene:
Linked Data
dbSNP Id:
rs1363008577
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551419C>G , CM000671.2:g.25551419C>G | GRCh38 |
| NC_000009.11:g.25551417C>G , CM000671.1:g.25551417C>G | GRCh37 |
| NC_000009.10:g.25541417C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-847G>C | ||
| XR_929525.2:n.674-847G>C |