Canonical Allele Identifier:
CA1475277614
Gene:
Linked Data
dbSNP Id:
rs1721484269
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89597844T>C , CM000666.2:g.89597844T>C | GRCh38 |
| NC_000004.11:g.90518995T>C , CM000666.1:g.90518995T>C | GRCh37 |
| NC_000004.10:g.90738018T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.298+9904T>C | ||
| XR_938987.1:n.433-309T>C | ||
| XR_938988.1:n.299-309T>C | ||
| XR_938990.1:n.298+9904T>C | ||
| XR_938991.1:n.298+9904T>C | ||
| XR_938992.1:n.298+9904T>C | ||
| XR_938994.1:n.643+9904T>C | ||
| XR_938995.1:n.477+9904T>C | ||
| XR_938996.1:n.298+9904T>C | ||
| XR_938997.1:n.298+9904T>C | ||
| XR_938986.2:n.323+9904T>C | ||
| XR_938987.2:n.493-309T>C |