Canonical Allele Identifier:
CA54965522
Gene:
Linked Data
dbSNP Id:
rs775610602
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122369246_122369247insCATA , CM000664.2:g.122369246_122369247insCATA | GRCh38 |
| NC_000002.11:g.123126822_123126823insCATA , CM000664.1:g.123126822_123126823insCATA | GRCh37 |
| NC_000002.10:g.122843292_122843293insCATA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-23717_556-23716insCATA | ||
| XR_001739684.1:n.556-23717_556-23716insCATA |