Canonical Allele Identifier:
CA1350284024
Gene:
Linked Data
dbSNP Id:
rs1698203676
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.21207127C>G , CM000665.2:g.21207127C>G | GRCh38 |
| NC_000003.11:g.21248619C>G , CM000665.1:g.21248619C>G | GRCh37 |
| NC_000003.10:g.21223623C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940646.1:n.254-3871C>G | ||
| XR_940646.2:n.547-3871C>G |