Canonical Allele Identifier:
CA1816081269
Gene:
Linked Data
dbSNP Id:
rs1814949267
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.122395979C>A , CM000670.2:g.122395979C>A | GRCh38 |
| NC_000008.10:g.123408218C>A , CM000670.1:g.123408218C>A | GRCh37 |
| NC_000008.9:g.123477399C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928599.1:n.152+3193G>T | ||
| XR_928599.3:n.152+3193G>T |