Canonical Allele Identifier:
CA2718947804
Gene:
Linked Data
dbSNP Id:
rs2117978862
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551568A>C , CM000671.2:g.25551568A>C | GRCh38 |
| NC_000009.11:g.25551566A>C , CM000671.1:g.25551566A>C | GRCh37 |
| NC_000009.10:g.25541566A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-996T>G | ||
| XR_929525.2:n.674-996T>G |