Canonical Allele Identifier: CA186000938

Gene: CCDC26

Linked Data

• dbSNP Id: rs188701761
• gnomAD v3: 8-129601264-C-T
• gnomAD v4: 8-129601264-C-T
• MyVariant Identifiers: chr8:g.130613510C>T (hg19) ; chr8:g.129601264C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601264C>T , CM000670.2:g.129601264C>T	GRCh38
NC_000008.10:g.130613510C>T , CM000670.1:g.130613510C>T	GRCh37
NC_000008.9:g.130682692C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78664G>A