Canonical Allele Identifier:
CA2008080828
Gene:
Linked Data
dbSNP Id:
rs10893872
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128455658T>G , CM000673.2:g.128455658T>G | GRCh38 |
| NC_000011.9:g.128325553T>G , CM000673.1:g.128325553T>G | GRCh37 |
| NC_000011.8:g.127830763T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948164.1:n.4378T>G | ||
| XR_948165.1:n.3467+911T>G |