Canonical Allele Identifier:
CA2698091720
Gene:
Linked Data
dbSNP Id:
rs2103116465
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.198500106A>G , CM000663.2:g.198500106A>G | GRCh38 |
| NC_000001.10:g.198469236A>G , CM000663.1:g.198469236A>G | GRCh37 |
| NC_000001.9:g.196735859A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922398.1:n.679+19445T>C | ||
| XR_922398.2:n.341+19445T>C |