Canonical Allele Identifier: CA596789674

Gene:

Linked Data

• dbSNP Id: rs3842250
• gnomAD v2: 11-636701-C-CG
• gnomAD v3: 11-636701-C-CG
• gnomAD v4: 11-636701-C-CG
• MyVariant Identifiers: chr11:g.636705_636706insG (hg19) ; chr11:g.636701_636702insG (hg19) ; chr11:g.636705_636706insG (hg38) ; chr11:g.636701_636702insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.636711dup , CM000673.2:g.636711dup	GRCh38
NC_000011.9:g.636711dup , CM000673.1:g.636711dup	GRCh37
NC_000011.8:g.626711dup	NCBI36
NG_021241.1:g.4407dup