Canonical Allele Identifier:
CA1267947427
Gene:
Linked Data
dbSNP Id:
rs1210898490
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88016234A>G , CM000664.2:g.88016234A>G | GRCh38 |
| NC_000002.11:g.88315753A>G , CM000664.1:g.88315753A>G | GRCh37 |
| NC_000002.10:g.88096868A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.579A>G | ||
| XR_940336.3:n.579A>G |