Canonical Allele Identifier:
CA1219564522
Gene:
Linked Data
dbSNP Id:
rs1659427265
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.201029479A>G , CM000663.2:g.201029479A>G | GRCh38 |
| NC_000001.10:g.200998607A>G , CM000663.1:g.200998607A>G | GRCh37 |
| NC_000001.9:g.199265230A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241170.3:n.423-1099A>G | ||
| XR_922405.1:n.961-1099A>G | ||
| XR_922406.1:n.1238+865A>G | ||
| XR_922407.1:n.1149-1099A>G | ||
| XR_922408.1:n.327-1099A>G | ||
| XR_922409.1:n.961-1099A>G | ||
| XR_922410.1:n.349-1099A>G | ||
| XR_922411.1:n.941-1099A>G | ||
| XR_922412.1:n.1154+865A>G | ||
| XR_922413.1:n.1050+865A>G | ||
| XR_922414.1:n.258-1099A>G | ||
| XR_922415.1:n.961-1099A>G | ||
| XR_922416.1:n.267-1099A>G | ||
| XR_922417.1:n.845-1099A>G | ||
| XR_922418.1:n.961-1099A>G | ||
| XR_922419.1:n.960+3860A>G | ||
| XR_922420.1:n.961-1099A>G | ||
| XR_001738364.1:n.609+865A>G | ||
| XR_001738365.1:n.520-1099A>G | ||
| XR_001738366.1:n.332-1099A>G | ||
| XR_001738367.1:n.525+865A>G | ||
| XR_001738368.1:n.421+865A>G | ||
| XR_001738369.1:n.332-1099A>G | ||
| XR_001738370.1:n.332-1099A>G | ||
| XR_001738371.1:n.331+3860A>G | ||
| XR_001738372.1:n.332-1099A>G | ||
| XR_922405.3:n.1071-1099A>G | ||
| XR_922407.3:n.1259-1099A>G | ||
| XR_922408.2:n.332-1099A>G | ||
| XR_922410.2:n.341-1099A>G | ||
| XR_922414.2:n.250-1099A>G | ||
| XR_922416.2:n.259-1099A>G | ||
| XR_922417.3:n.955-1099A>G |