Canonical Allele Identifier:
CA101489350
Gene:
Linked Data
dbSNP Id:
rs981409889
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89655827A>T , CM000666.2:g.89655827A>T | GRCh38 |
| NC_000004.11:g.90576978A>T , CM000666.1:g.90576978A>T | GRCh37 |
| NC_000004.10:g.90796001A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.434+27910A>T | ||
| XR_938987.1:n.688+27910A>T | ||
| XR_938988.1:n.554+27910A>T | ||
| XR_938990.1:n.299-35458A>T | ||
| XR_938991.1:n.434+27910A>T | ||
| XR_938994.1:n.779+27910A>T | ||
| XR_938995.1:n.613+27910A>T | ||
| XR_938986.2:n.459+27910A>T | ||
| XR_938987.2:n.748+27910A>T |