Canonical Allele Identifier:
CA2485998819
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.213737151T>C , CM000663.2:g.213737151T>C | GRCh38 |
| NC_000001.10:g.213910494T>C , CM000663.1:g.213910494T>C | GRCh37 |
| NC_000001.9:g.211977117T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922586.1:n.136+5593T>C | ||
| XR_922587.1:n.136+5593T>C | ||
| XR_001738463.1:n.742+5593T>C | ||
| XR_001738464.1:n.567+5593T>C |