Canonical Allele Identifier:
CA1475277702
Gene:
Linked Data
dbSNP Id:
rs961780198
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89598012A>C , CM000666.2:g.89598012A>C | GRCh38 |
| NC_000004.11:g.90519163A>C , CM000666.1:g.90519163A>C | GRCh37 |
| NC_000004.10:g.90738186A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.298+10072A>C | ||
| XR_938987.1:n.433-141A>C | ||
| XR_938988.1:n.299-141A>C | ||
| XR_938990.1:n.298+10072A>C | ||
| XR_938991.1:n.298+10072A>C | ||
| XR_938992.1:n.298+10072A>C | ||
| XR_938994.1:n.643+10072A>C | ||
| XR_938995.1:n.477+10072A>C | ||
| XR_938996.1:n.298+10072A>C | ||
| XR_938997.1:n.298+10072A>C | ||
| XR_938986.2:n.323+10072A>C | ||
| XR_938987.2:n.493-141A>C |