Canonical Allele Identifier:
CA1439212609
Gene:
Linked Data
dbSNP Id:
rs1711579854
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12577993G>A , CM000666.2:g.12577993G>A | GRCh38 |
| NC_000004.11:g.12579617G>A , CM000666.1:g.12579617G>A | GRCh37 |
| NC_000004.10:g.12188715G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+31349C>T | ||
| XR_001741374.1:n.254+44662C>T | ||
| XR_925406.3:n.140+31349C>T |