Canonical Allele Identifier:
CA1284674311
Gene:
Linked Data
dbSNP Id:
rs1680376115
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122884144G>A , CM000664.2:g.122884144G>A | GRCh38 |
| NC_000002.11:g.123641720G>A , CM000664.1:g.123641720G>A | GRCh37 |
| NC_000002.10:g.123358190G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-798G>A | ||
| XR_001739692.1:n.1451-798G>A | ||
| XR_923292.2:n.1358-798G>A |