Canonical Allele Identifier:
CA1912720936
Gene:
Linked Data
dbSNP Id:
rs1839462263
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.57812932C>T , CM000672.2:g.57812932C>T | GRCh38 |
| NC_000010.10:g.59572692C>T , CM000672.1:g.59572692C>T | GRCh37 |
| NC_000010.9:g.59242698C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945979.1:n.68+34360G>A | ||
| XR_001747454.1:n.85+34360G>A |