Canonical Allele Identifier:
CA1284674357
Gene:
Linked Data
dbSNP Id:
rs1680376871
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122884201T>G , CM000664.2:g.122884201T>G | GRCh38 |
| NC_000002.11:g.123641777T>G , CM000664.1:g.123641777T>G | GRCh37 |
| NC_000002.10:g.123358247T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-741T>G | ||
| XR_001739692.1:n.1451-741T>G | ||
| XR_923292.2:n.1358-741T>G |