Canonical Allele Identifier: CA585157827

Gene: CCDC26

Linked Data

• dbSNP Id: rs1307953159
• gnomAD v2: 8-130572164-C-A
• gnomAD v3: 8-129559918-C-A
• gnomAD v4: 8-129559918-C-A
• MyVariant Identifiers: chr8:g.130572164C>A (hg19) ; chr8:g.129559918C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559918C>A , CM000670.2:g.129559918C>A	GRCh38
NC_000008.10:g.130572164C>A , CM000670.1:g.130572164C>A	GRCh37
NC_000008.9:g.130641346C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79228G>T
NR_130918.1:n.137+14964G>T
NR_130919.1:n.137+14964G>T
NR_130920.1:n.137+14964G>T