Canonical Allele Identifier:
CA2332763279
Gene:
Linked Data
dbSNP Id:
rs1370592438
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521971A>G , CM000681.2:g.33521971A>G | GRCh38 |
| NC_000019.9:g.34012877A>G , CM000681.1:g.34012877A>G | GRCh37 |
| NC_000019.8:g.38704717A>G | NCBI36 |
| NG_013358.1:g.4923T>C | |
| NG_013358.2:g.4923T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.30A>G | ||
| XR_935919.1:n.25A>G | ||
| XR_001754035.2:n.38A>G | ||
| XR_935918.2:n.38A>G |