Canonical Allele Identifier:
CA2298481285
Gene:
Linked Data
dbSNP Id:
rs1910119829
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.41477777T>C , CM000680.2:g.41477777T>C | GRCh38 |
| NC_000018.9:g.39057741T>C , CM000680.1:g.39057741T>C | GRCh37 |
| NC_000018.8:g.37311739T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_935409.1:n.86-26357T>C |