Canonical Allele Identifier:
CA799758183
Gene:
Linked Data
dbSNP Id:
rs1356773690
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89597827C>T , CM000666.2:g.89597827C>T | GRCh38 |
| NC_000004.11:g.90518978C>T , CM000666.1:g.90518978C>T | GRCh37 |
| NC_000004.10:g.90738001C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.298+9887C>T | ||
| XR_938987.1:n.433-326C>T | ||
| XR_938988.1:n.299-326C>T | ||
| XR_938990.1:n.298+9887C>T | ||
| XR_938991.1:n.298+9887C>T | ||
| XR_938992.1:n.298+9887C>T | ||
| XR_938994.1:n.643+9887C>T | ||
| XR_938995.1:n.477+9887C>T | ||
| XR_938996.1:n.298+9887C>T | ||
| XR_938997.1:n.298+9887C>T | ||
| XR_938986.2:n.323+9887C>T | ||
| XR_938987.2:n.493-326C>T |