Canonical Allele Identifier: CA847371697

Gene: CCDC26

Linked Data

• dbSNP Id: rs1348225303
• gnomAD v3: 8-129559878-T-C
• gnomAD v4: 8-129559878-T-C
• MyVariant Identifiers: chr8:g.130572124T>C (hg19) ; chr8:g.129559878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559878T>C , CM000670.2:g.129559878T>C	GRCh38
NC_000008.10:g.130572124T>C , CM000670.1:g.130572124T>C	GRCh37
NC_000008.9:g.130641306T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79188A>G
NR_130918.1:n.137+15004A>G
NR_130919.1:n.137+15004A>G
NR_130920.1:n.137+15004A>G