Linked Data
dbSNP Id:
rs1565236810
gnomAD v2:
11-62622884-G-GT
gnomAD v3:
11-62855412-G-GT
gnomAD v4:
11-62855412-G-GT
MyVariant Identifiers:
chr11:g.62622884_62622885insT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.62855413dup , CM000673.2:g.62855413dup | GRCh38 |
| NC_000011.9:g.62622885dup , CM000673.1:g.62622885dup | GRCh37 |
| NC_000011.8:g.62379461dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003098.1:n.67+11dup | ||
| NR_003098.2:n.64+11dup | ||
| NR_152575.1:n.462+11dup | ||
| NR_152576.1:n.462+11dup | ||
| NR_152577.1:n.64+11dup | ||
| NR_152578.1:n.22-197dup | ||
| NR_152579.1:n.64+11dup | ||
| NR_152580.1:n.64+11dup | ||
| NR_152581.1:n.64+11dup | ||
| NR_152582.1:n.22-197dup | ||
| NR_152583.1:n.64+11dup | ||
| NR_152584.1:n.462+11dup | ||
| NR_152585.1:n.462+11dup |