Canonical Allele Identifier: CA186000970

Gene: CCDC26

Linked Data

• dbSNP Id: rs571476990
• gnomAD v2: 8-130613739-T-A
• gnomAD v3: 8-129601493-T-A
• gnomAD v4: 8-129601493-T-A
• MyVariant Identifiers: chr8:g.130613739T>A (hg19) ; chr8:g.129601493T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601493T>A , CM000670.2:g.129601493T>A	GRCh38
NC_000008.10:g.130613739T>A , CM000670.1:g.130613739T>A	GRCh37
NC_000008.9:g.130682921T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78435A>T