Canonical Allele Identifier:
CA1267947193
Gene:
Linked Data
dbSNP Id:
rs1351829777
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88015971C>T , CM000664.2:g.88015971C>T | GRCh38 |
| NC_000002.11:g.88315490C>T , CM000664.1:g.88315490C>T | GRCh37 |
| NC_000002.10:g.88096605C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.316C>T | ||
| XR_940336.3:n.316C>T |