Canonical Allele Identifier:
CA2735630919
Gene:
Linked Data
dbSNP Id:
rs987635528
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521963G>C , CM000681.2:g.33521963G>C | GRCh38 |
| NC_000019.9:g.34012869G>C , CM000681.1:g.34012869G>C | GRCh37 |
| NC_000019.8:g.38704709G>C | NCBI36 |
| NG_013358.1:g.4931C>G | |
| NG_013358.2:g.4931C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.22G>C | ||
| XR_935919.1:n.17G>C | ||
| XR_001754035.2:n.30G>C | ||
| XR_935918.2:n.30G>C |