Canonical Allele Identifier: CA185985533

Gene: CCDC26

Linked Data

• dbSNP Id: rs773223626
• MyVariant Identifiers: chr8:g.130477778del (hg19) ; chr8:g.129465532del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129465532del , CM000670.2:g.129465532del	GRCh38
NC_000008.10:g.130477778del , CM000670.1:g.130477778del	GRCh37
NC_000008.9:g.130546960del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.360+15111del
NR_130918.1:n.138-95155del
NR_130919.1:n.138-65848del
NR_130920.1:n.138-65848del