Canonical Allele Identifier: CA847373338

Gene: CCDC26

Linked Data

• dbSNP Id: rs1184817719
• MyVariant Identifiers: chr8:g.130477820del (hg19) ; chr8:g.129465574del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129465575del , CM000670.2:g.129465575del	GRCh38
NC_000008.10:g.130477821del , CM000670.1:g.130477821del	GRCh37
NC_000008.9:g.130547003del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.360+15069del
NR_130918.1:n.138-95197del
NR_130919.1:n.138-65890del
NR_130920.1:n.138-65890del