Canonical Allele Identifier:
CA1800979889
Gene:
Linked Data
dbSNP Id:
rs1808585999
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.88981219A>C , CM000670.2:g.88981219A>C | GRCh38 |
| NC_000008.10:g.89993448A>C , CM000670.1:g.89993448A>C | GRCh37 |
| NC_000008.9:g.90062564A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_002956667.1:n.179-99158T>G |