Canonical Allele Identifier: CA186000931

Gene: CCDC26

Linked Data

• dbSNP Id: rs144724361
• gnomAD v2: 8-130613469-G-T
• gnomAD v3: 8-129601223-G-T
• gnomAD v4: 8-129601223-G-T
• MyVariant Identifiers: chr8:g.130613469G>T (hg19) ; chr8:g.129601223G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601223G>T , CM000670.2:g.129601223G>T	GRCh38
NC_000008.10:g.130613469G>T , CM000670.1:g.130613469G>T	GRCh37
NC_000008.9:g.130682651G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78705C>A