Canonical Allele Identifier:
CA2733190172
Gene:
Linked Data
dbSNP Id:
rs2151857671
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8137779_8137780insTTAC , CM000679.2:g.8137779_8137780insTTAC | GRCh38 |
| NC_000017.10:g.8041097_8041098insTTAC , CM000679.1:g.8041097_8041098insTTAC | GRCh37 |
| NC_000017.9:g.7981822_7981823insTTAC | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934202.1:n.183-1070_183-1069insTTAC | ||
| XR_934203.1:n.70-1698_70-1697insTTAC | ||
| XR_934202.2:n.414-1070_414-1069insTTAC |