Canonical Allele Identifier:
CA2369443224
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.52408842A>T , CM000682.2:g.52408842A>T | GRCh38 |
| NC_000020.10:g.51025381A>T , CM000682.1:g.51025381A>T | GRCh37 |
| NC_000020.9:g.50458788A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001754670.1:n.434+68190A>T | ||
| XR_001754671.1:n.434+68190A>T | ||
| XR_002958559.1:n.471+68190A>T |