Canonical Allele Identifier:
CA721212395
Gene:
Linked Data
dbSNP Id:
rs1170727149
gnomAD v3:
16-49108500-T-TTAC
gnomAD v4:
16-49108500-T-TTAC
MyVariant Identifiers:
chr16:g.49142411_49142412insTAC (hg19)
chr16:g.49108500_49108501insTAC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.49108506_49108508dup , CM000678.2:g.49108506_49108508dup | GRCh38 |
| NC_000016.9:g.49142417_49142419dup , CM000678.1:g.49142417_49142419dup | GRCh37 |
| NC_000016.8:g.47699918_47699920dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_933517.1:n.810+1441_810+1443dup | ||
| XR_001752138.2:n.591+5473_591+5475dup | ||
| XR_933517.2:n.810+1441_810+1443dup |