Canonical Allele Identifier:
CA2725210665
Gene:
Linked Data
dbSNP Id:
rs2135970825
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128870922G>C , CM000673.2:g.128870922G>C | GRCh38 |
| NC_000011.9:g.128740817G>C , CM000673.1:g.128740817G>C | GRCh37 |
| NC_000011.8:g.128246027G>C | NCBI36 |
| NG_009379.1:g.1452C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948172.1:n.5989C>G | ||
| XR_948173.1:n.5678C>G |