Canonical Allele Identifier:
CA2700016175
Gene:
Linked Data
dbSNP Id:
rs2104588595
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88016330A>C , CM000664.2:g.88016330A>C | GRCh38 |
| NC_000002.11:g.88315849A>C , CM000664.1:g.88315849A>C | GRCh37 |
| NC_000002.10:g.88096964A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.675A>C | ||
| XR_940336.3:n.675A>C |