Linked Data
dbSNP Id:
rs1297389997
MyVariant Identifiers:
chr2:g.61091867_61091868insACACAG (hg19)
chr2:g.60864732_60864733insACACAG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.60864741_60864746dup , CM000664.2:g.60864741_60864746dup | GRCh38 |
| NC_000002.11:g.61091876_61091881dup , CM000664.1:g.61091876_61091881dup | GRCh37 |
| NC_000002.10:g.60945380_60945385dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_033980.1:n.84-7818_84-7813dup |