Canonical Allele Identifier:
CA1609069920
Gene:
Linked Data
dbSNP Id:
rs1765600134
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.8525106G>A , CM000668.2:g.8525106G>A | GRCh38 |
| NC_000006.11:g.8525339G>A , CM000668.1:g.8525339G>A | GRCh37 |
| NC_000006.10:g.8470338G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_038979.1:n.626-33479G>A | ||
| NR_038980.1:n.649-33479G>A |