Canonical Allele Identifier:
CA1218511596
Gene:
Linked Data
dbSNP Id:
rs1658971031
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.198500132G>C , CM000663.2:g.198500132G>C | GRCh38 |
| NC_000001.10:g.198469262G>C , CM000663.1:g.198469262G>C | GRCh37 |
| NC_000001.9:g.196735885G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922398.1:n.679+19419C>G | ||
| XR_922398.2:n.341+19419C>G |