Canonical Allele Identifier: CA98770167

Gene:

Linked Data

• dbSNP Id: rs943378470
• gnomAD v2: 4-69659673-C-CT
• gnomAD v3: 4-68793955-C-CT
• gnomAD v4: 4-68793955-C-CT
• MyVariant Identifiers: chr4:g.69659674_69659675insT (hg19) ; chr4:g.69659673_69659674insT (hg19) ; chr4:g.68793956_68793957insT (hg38) ; chr4:g.68793955_68793956insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68793961dup , CM000666.2:g.68793961dup	GRCh38
NC_000004.11:g.69659679dup , CM000666.1:g.69659679dup	GRCh37
NC_000004.10:g.69694268dup	NCBI36