Canonical Allele Identifier:
CA1870932957
Gene:
Linked Data
dbSNP Id:
rs1826974454
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.108092833A>G , CM000671.2:g.108092833A>G | GRCh38 |
| NC_000009.11:g.110855114A>G , CM000671.1:g.110855114A>G | GRCh37 |
| NC_000009.10:g.109894935A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930239.1:n.461-39539T>C | ||
| XR_001746881.1:n.668-39539T>C | ||
| XR_001746882.1:n.668-39539T>C |