Canonical Allele Identifier:
CA853715733
Gene:
Linked Data
dbSNP Id:
rs1404378807
MyVariant Identifiers:
chr8:g.5765042_5765043insGGAGAAGAG (hg19)
chr8:g.5907520_5907521insGGAGAAGAG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.5907531_5907539dup , CM000670.2:g.5907531_5907539dup | GRCh38 |
| NC_000008.10:g.5765053_5765061dup , CM000670.1:g.5765053_5765061dup | GRCh37 |
| NC_000008.9:g.5752461_5752469dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_941374.1:n.308-7798_308-7790dup | ||
| XR_941375.1:n.308-7798_308-7790dup | ||
| XR_941376.1:n.406-7798_406-7790dup | ||
| XR_941377.1:n.308-7798_308-7790dup | ||
| XR_941378.1:n.216-7798_216-7790dup | ||
| XR_001745765.1:n.308-7798_308-7790dup | ||
| XR_001745766.1:n.406-7798_406-7790dup | ||
| XR_001745767.1:n.216-7798_216-7790dup | ||
| XR_001745768.1:n.308-7798_308-7790dup | ||
| XR_941374.2:n.308-7798_308-7790dup | ||
| XR_941375.2:n.308-7798_308-7790dup |