Canonical Allele Identifier:
CA1284674121
Gene:
Linked Data
dbSNP Id:
rs1680372665
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122883956C>A , CM000664.2:g.122883956C>A | GRCh38 |
| NC_000002.11:g.123641532C>A , CM000664.1:g.123641532C>A | GRCh37 |
| NC_000002.10:g.123358002C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-986C>A | ||
| XR_001739692.1:n.1451-986C>A | ||
| XR_923292.2:n.1358-986C>A |