Canonical Allele Identifier:
CA2246165898
Gene:
Linked Data
dbSNP Id:
rs1981893690
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8137575T>C , CM000679.2:g.8137575T>C | GRCh38 |
| NC_000017.10:g.8040893T>C , CM000679.1:g.8040893T>C | GRCh37 |
| NC_000017.9:g.7981618T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934202.1:n.183-1274T>C | ||
| XR_934203.1:n.70-1902T>C | ||
| XR_934202.2:n.414-1274T>C |