Canonical Allele Identifier:
CA1816697734
Gene:
Linked Data
dbSNP Id:
rs1814529971
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.123753541T>G , CM000670.2:g.123753541T>G | GRCh38 |
| NC_000008.10:g.124765781T>G , CM000670.1:g.124765781T>G | GRCh37 |
| NC_000008.9:g.124834962T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928607.1:n.153-11242T>G | ||
| XR_928607.3:n.324-11242T>G |