Canonical Allele Identifier:
CA2700304560
Gene:
Linked Data
dbSNP Id:
rs2104681829
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122369225_122369226insCGAT , CM000664.2:g.122369225_122369226insCGAT | GRCh38 |
| NC_000002.11:g.123126801_123126802insCGAT , CM000664.1:g.123126801_123126802insCGAT | GRCh37 |
| NC_000002.10:g.122843271_122843272insCGAT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-23738_556-23737insCGAT | ||
| XR_001739684.1:n.556-23738_556-23737insCGAT |