Canonical Allele Identifier:
CA1760507829
Gene:
Linked Data
dbSNP Id:
rs1798580887
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.5907522G>C , CM000670.2:g.5907522G>C | GRCh38 |
| NC_000008.10:g.5765044G>C , CM000670.1:g.5765044G>C | GRCh37 |
| NC_000008.9:g.5752452G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_941374.1:n.308-7791C>G | ||
| XR_941375.1:n.308-7791C>G | ||
| XR_941376.1:n.406-7791C>G | ||
| XR_941377.1:n.308-7791C>G | ||
| XR_941378.1:n.216-7791C>G | ||
| XR_001745765.1:n.308-7791C>G | ||
| XR_001745766.1:n.406-7791C>G | ||
| XR_001745767.1:n.216-7791C>G | ||
| XR_001745768.1:n.308-7791C>G | ||
| XR_941374.2:n.308-7791C>G | ||
| XR_941375.2:n.308-7791C>G |