Canonical Allele Identifier: CA185985536

Gene: CCDC26

Linked Data

• dbSNP Id: rs909274753
• gnomAD v3: 8-129465559-G-A
• gnomAD v4: 8-129465559-G-A
• MyVariant Identifiers: chr8:g.130477805G>A (hg19) ; chr8:g.129465559G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129465559G>A , CM000670.2:g.129465559G>A	GRCh38
NC_000008.10:g.130477805G>A , CM000670.1:g.130477805G>A	GRCh37
NC_000008.9:g.130546987G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.360+15084C>T
NR_130918.1:n.138-95182C>T
NR_130919.1:n.138-65875C>T
NR_130920.1:n.138-65875C>T