Canonical Allele Identifier: CA186000956

Gene: CCDC26

Linked Data

• dbSNP Id: rs959365514
• MyVariant Identifiers: chr8:g.130613677G>A (hg19) ; chr8:g.129601431G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601431G>A , CM000670.2:g.129601431G>A	GRCh38
NC_000008.10:g.130613677G>A , CM000670.1:g.130613677G>A	GRCh37
NC_000008.9:g.130682859G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78497C>T