Canonical Allele Identifier:
CA1427629927
Gene:
Linked Data
dbSNP Id:
rs1165963583
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.187931593T>C , CM000665.2:g.187931593T>C | GRCh38 |
| NC_000003.11:g.187649381T>C , CM000665.1:g.187649381T>C | GRCh37 |
| NC_000003.10:g.189132075T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_924814.1:n.1321A>G |