Canonical Allele Identifier:
CA1769199299
Gene:
Linked Data
dbSNP Id:
rs2071238885
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.20130027T>G , CM000670.2:g.20130027T>G | GRCh38 |
| NC_000008.10:g.19987538T>G , CM000670.1:g.19987538T>G | GRCh37 |
| NC_000008.9:g.20031818T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_949563.1:n.3408+108T>G | ||
| XR_949563.2:n.3400+108T>G |