Canonical Allele Identifier:
CA2246165892
Gene:
Linked Data
dbSNP Id:
rs1981893534
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8137571C>G , CM000679.2:g.8137571C>G | GRCh38 |
| NC_000017.10:g.8040889C>G , CM000679.1:g.8040889C>G | GRCh37 |
| NC_000017.9:g.7981614C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934202.1:n.183-1278C>G | ||
| XR_934203.1:n.70-1906C>G | ||
| XR_934202.2:n.414-1278C>G |