Canonical Allele Identifier: CA1119137290

Gene: CCDC26

Linked Data

• dbSNP Id: rs1820171771
• gnomAD v3: 8-129465541-A-C
• gnomAD v4: 8-129465541-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129465541A>C , CM000670.2:g.129465541A>C	GRCh38
NC_000008.10:g.130477787A>C , CM000670.1:g.130477787A>C	GRCh37
NC_000008.9:g.130546969A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.360+15102T>G
NR_130918.1:n.138-95164T>G
NR_130919.1:n.138-65857T>G
NR_130920.1:n.138-65857T>G