Canonical Allele Identifier:
CA1403911659
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.135506407T>C , CM000665.2:g.135506407T>C | GRCh38 |
| NC_000003.11:g.135225249T>C , CM000665.1:g.135225249T>C | GRCh37 |
| NC_000003.10:g.136707939T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_924527.1:n.225+9743A>G | ||
| XR_924528.1:n.225+9743A>G | ||
| XR_001740926.1:n.229+9743A>G | ||
| XR_002959651.1:n.229+9743A>G | ||
| XR_924527.3:n.229+9743A>G | ||
| XR_924528.3:n.229+9743A>G |