Canonical Allele Identifier:
CA2255111824
Gene:
Linked Data
dbSNP Id:
rs1597650222
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237151T>C , CM000679.2:g.30237151T>C | GRCh38 |
| NC_000017.10:g.28564169T>C , CM000679.1:g.28564169T>C | GRCh37 |
| NC_000017.9:g.25588295T>C | NCBI36 |
| NG_011747.2:g.3786A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.165+81T>C | ||
| XR_001752824.1:n.280+81T>C |