Canonical Allele Identifier:
CA2706428985
Gene:
Linked Data
dbSNP Id:
rs2110111229
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89597826C>G , CM000666.2:g.89597826C>G | GRCh38 |
| NC_000004.11:g.90518977C>G , CM000666.1:g.90518977C>G | GRCh37 |
| NC_000004.10:g.90738000C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.298+9886C>G | ||
| XR_938987.1:n.433-327C>G | ||
| XR_938988.1:n.299-327C>G | ||
| XR_938990.1:n.298+9886C>G | ||
| XR_938991.1:n.298+9886C>G | ||
| XR_938992.1:n.298+9886C>G | ||
| XR_938994.1:n.643+9886C>G | ||
| XR_938995.1:n.477+9886C>G | ||
| XR_938996.1:n.298+9886C>G | ||
| XR_938997.1:n.298+9886C>G | ||
| XR_938986.2:n.323+9886C>G | ||
| XR_938987.2:n.493-327C>G |