Canonical Allele Identifier: CA186004579

Gene: CCDC26

Linked Data

• dbSNP Id: rs139834653
• gnomAD v2: 8-130645687-C-CT
• gnomAD v3: 8-129633441-C-CT
• gnomAD v4: 8-129633441-C-CT
• MyVariant Identifiers: chr8:g.130645687_130645688insT (hg19) ; chr8:g.129633441_129633442insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129633442dup , CM000670.2:g.129633442dup	GRCh38
NC_000008.10:g.130645688dup , CM000670.1:g.130645688dup	GRCh37
NC_000008.9:g.130714870dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+46486dup