Canonical Allele Identifier:
CA1817437343
Gene:
Linked Data
dbSNP Id:
rs1815192162
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.125474199A>T , CM000670.2:g.125474199A>T | GRCh38 |
| NC_000008.10:g.126486441A>T , CM000670.1:g.126486441A>T | GRCh37 |
| NC_000008.9:g.126555623A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928628.1:n.256+885A>T |