Canonical Allele Identifier:
CA1839056722
Gene:
Linked Data
dbSNP Id:
rs1823378621
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21756046C>G , CM000671.2:g.21756046C>G | GRCh38 |
| NC_000009.11:g.21756045C>G , CM000671.1:g.21756045C>G | GRCh37 |
| NC_000009.10:g.21746045C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001746563.2:n.163+11779G>C |