Canonical Allele Identifier: CA185996164

Gene: CCDC26

Linked Data

• dbSNP Id: rs758558614
• MyVariant Identifiers: chr8:g.130572209del (hg19) ; chr8:g.129559963del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559963del , CM000670.2:g.129559963del	GRCh38
NC_000008.10:g.130572209del , CM000670.1:g.130572209del	GRCh37
NC_000008.9:g.130641391del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79273del
NR_130918.1:n.137+14919del
NR_130919.1:n.137+14919del
NR_130920.1:n.137+14919del