Canonical Allele Identifier: CA186004567

Gene: CCDC26

Linked Data

• dbSNP Id: rs575417830
• gnomAD v2: 8-130645591-G-GA
• gnomAD v3: 8-129633345-G-GA
• gnomAD v4: 8-129633345-G-GA
• MyVariant Identifiers: chr8:g.130645591_130645592insA (hg19) ; chr8:g.129633345_129633346insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129633351dup , CM000670.2:g.129633351dup	GRCh38
NC_000008.10:g.130645597dup , CM000670.1:g.130645597dup	GRCh37
NC_000008.9:g.130714779dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_130917.1:n.312+46582dup