Canonical Allele Identifier: CA12740316

Gene: CCDC26

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129611859G>C , CM000670.2:g.129611859G>C	GRCh38
NC_000008.10:g.130624105G>C , CM000670.1:g.130624105G>C	GRCh37
NC_000008.9:g.130693287G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+68069C>G