Canonical Allele Identifier: CA185996150

Gene: CCDC26

Linked Data

• dbSNP Id: rs562299655
• gnomAD v3: 8-129559827-C-T
• gnomAD v4: 8-129559827-C-T
• MyVariant Identifiers: chr8:g.130572073C>T (hg19) ; chr8:g.129559827C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559827C>T , CM000670.2:g.129559827C>T	GRCh38
NC_000008.10:g.130572073C>T , CM000670.1:g.130572073C>T	GRCh37
NC_000008.9:g.130641255C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79137G>A
NR_130918.1:n.137+15055G>A
NR_130919.1:n.137+15055G>A
NR_130920.1:n.137+15055G>A