Linked Data
dbSNP Id:
rs1374377808
MyVariant Identifiers:
chr2:g.61091897_61091898insAAAGACC (hg19)
chr2:g.60864762_60864763insAAAGACC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.60864764_60864770dup , CM000664.2:g.60864764_60864770dup | GRCh38 |
| NC_000002.11:g.61091899_61091905dup , CM000664.1:g.61091899_61091905dup | GRCh37 |
| NC_000002.10:g.60945403_60945409dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_033980.1:n.84-7849_84-7843dup |