Canonical Allele Identifier: CA186004573

Gene: CCDC26

Linked Data

• dbSNP Id: rs907981561
• MyVariant Identifiers: chr8:g.130645648A>T (hg19) ; chr8:g.129633402A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129633402A>T , CM000670.2:g.129633402A>T	GRCh38
NC_000008.10:g.130645648A>T , CM000670.1:g.130645648A>T	GRCh37
NC_000008.9:g.130714830A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_130917.1:n.312+46526T>A