Canonical Allele Identifier: CA186004593

Gene: CCDC26

Linked Data

• dbSNP Id: rs904834705
• gnomAD v3: 8-129633522-A-G
• gnomAD v4: 8-129633522-A-G
• MyVariant Identifiers: chr8:g.130645768A>G (hg19) ; chr8:g.129633522A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129633522A>G , CM000670.2:g.129633522A>G	GRCh38
NC_000008.10:g.130645768A>G , CM000670.1:g.130645768A>G	GRCh37
NC_000008.9:g.130714950A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_130917.1:n.312+46406T>C