Canonical Allele Identifier: CA185309925

Gene: CCDC26

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129673211T>G , CM000670.2:g.129673211T>G	GRCh38
NC_000008.10:g.130685457T>G , CM000670.1:g.130685457T>G	GRCh37
NC_000008.9:g.130754639T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+6717A>C