Canonical Allele Identifier:
CA1475277679
Gene:
Linked Data
dbSNP Id:
rs1721487266
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89597976A>G , CM000666.2:g.89597976A>G | GRCh38 |
| NC_000004.11:g.90519127A>G , CM000666.1:g.90519127A>G | GRCh37 |
| NC_000004.10:g.90738150A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.298+10036A>G | ||
| XR_938987.1:n.433-177A>G | ||
| XR_938988.1:n.299-177A>G | ||
| XR_938990.1:n.298+10036A>G | ||
| XR_938991.1:n.298+10036A>G | ||
| XR_938992.1:n.298+10036A>G | ||
| XR_938994.1:n.643+10036A>G | ||
| XR_938995.1:n.477+10036A>G | ||
| XR_938996.1:n.298+10036A>G | ||
| XR_938997.1:n.298+10036A>G | ||
| XR_938986.2:n.323+10036A>G | ||
| XR_938987.2:n.493-177A>G |