Canonical Allele Identifier: CA186000945

Gene: CCDC26

Linked Data

• dbSNP Id: rs896530624
• MyVariant Identifiers: chr8:g.130613596T>C (hg19) ; chr8:g.129601350T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601350T>C , CM000670.2:g.129601350T>C	GRCh38
NC_000008.10:g.130613596T>C , CM000670.1:g.130613596T>C	GRCh37
NC_000008.9:g.130682778T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78578A>G