Linked Data
dbSNP Id:
rs1258627329
gnomAD v2:
11-113346195-A-AG
gnomAD v3:
11-113475473-A-AG
gnomAD v4:
11-113475473-A-AG
MyVariant Identifiers:
chr11:g.113346195_113346196insG (hg19)
chr11:g.113475473_113475474insG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.113475475dup , CM000673.2:g.113475475dup | GRCh38 |
| NC_000011.9:g.113346197dup , CM000673.1:g.113346197dup | GRCh37 |
| NC_000011.8:g.112851407dup | NCBI36 |
| NG_008841.1:g.4806dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000540600.5:n.34+184dup |