Canonical Allele Identifier:
CA1596629088
Gene:
Linked Data
dbSNP Id:
rs1756514917
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.162656518T>G , CM000667.2:g.162656518T>G | GRCh38 |
| NC_000005.9:g.162083524T>G , CM000667.1:g.162083524T>G | GRCh37 |
| NC_000005.8:g.162016102T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001742958.1:n.418+3584A>C |