Canonical Allele Identifier: CA185985523

Gene: CCDC26

Linked Data

• dbSNP Id: rs34016364
• MyVariant Identifiers: chr8:g.130477671_130477672insA (hg19) ; chr8:g.129465425_129465426insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129465425_129465426insA , CM000670.2:g.129465425_129465426insA	GRCh38
NC_000008.10:g.130477671_130477672insA , CM000670.1:g.130477671_130477672insA	GRCh37
NC_000008.9:g.130546853_130546854insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.360+15217_360+15218insT
NR_130918.1:n.138-95049_138-95048insT
NR_130919.1:n.138-65742_138-65741insT
NR_130920.1:n.138-65742_138-65741insT