Canonical Allele Identifier: CA186000944

Gene: CCDC26

Linked Data

• dbSNP Id: rs901083781
• gnomAD v2: 8-130613593-AT-A
• gnomAD v3: 8-129601347-AT-A
• gnomAD v4: 8-129601347-AT-A
• MyVariant Identifiers: chr8:g.130613594del (hg19) ; chr8:g.129601348del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601356del , CM000670.2:g.129601356del	GRCh38
NC_000008.10:g.130613602del , CM000670.1:g.130613602del	GRCh37
NC_000008.9:g.130682784del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78580del