Canonical Allele Identifier: CA847373296

Gene: CCDC26

Linked Data

• dbSNP Id: rs1484996468
• gnomAD v3: 8-129465517-T-C
• gnomAD v4: 8-129465517-T-C
• MyVariant Identifiers: chr8:g.130477763T>C (hg19) ; chr8:g.129465517T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129465517T>C , CM000670.2:g.129465517T>C	GRCh38
NC_000008.10:g.130477763T>C , CM000670.1:g.130477763T>C	GRCh37
NC_000008.9:g.130546945T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.360+15126A>G
NR_130918.1:n.138-95140A>G
NR_130919.1:n.138-65833A>G
NR_130920.1:n.138-65833A>G