Canonical Allele Identifier: CA607758113

Gene:

Linked Data

• dbSNP Id: rs34541078
• gnomAD v2: 12-116211914-C-CT
• gnomAD v3: 12-115774109-C-CT
• gnomAD v4: 12-115774109-C-CT
• MyVariant Identifiers: chr12:g.116211919_116211920insT (hg19) ; chr12:g.116211914_116211915insT (hg19) ; chr12:g.115774114_115774115insT (hg38) ; chr12:g.115774109_115774110insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115774132dup , CM000674.2:g.115774132dup	GRCh38
NC_000012.11:g.116211937dup , CM000674.1:g.116211937dup	GRCh37
NC_000012.10:g.114696320dup	NCBI36