Canonical Allele Identifier:
CA1462694207
Gene:
Linked Data
dbSNP Id:
rs1756226765
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.62558089T>C , CM000666.2:g.62558089T>C | GRCh38 |
| NC_000004.11:g.63423807T>C , CM000666.1:g.63423807T>C | GRCh37 |
| NC_000004.10:g.63106402T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938814.1:n.161-5755T>C |