Canonical Allele Identifier: CA185996200

Gene: CCDC26

Linked Data

• dbSNP Id: rs901765456
• MyVariant Identifiers: chr8:g.129560218A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129560218A>T , CM000670.2:g.129560218A>T	GRCh38
NC_000008.10:g.130572464A>T , CM000670.1:g.130572464A>T	GRCh37
NC_000008.9:g.130641646A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79528T>A
NR_130918.1:n.137+14664T>A
NR_130919.1:n.137+14664T>A
NR_130920.1:n.137+14664T>A