Canonical Allele Identifier: CA186004559

Gene: CCDC26

Linked Data

• dbSNP Id: rs543216029
• gnomAD v2: 8-130645557-A-C
• gnomAD v3: 8-129633311-A-C
• gnomAD v4: 8-129633311-A-C
• MyVariant Identifiers: chr8:g.130645557A>C (hg19) ; chr8:g.129633311A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129633311A>C , CM000670.2:g.129633311A>C	GRCh38
NC_000008.10:g.130645557A>C , CM000670.1:g.130645557A>C	GRCh37
NC_000008.9:g.130714739A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+46617T>G