Canonical Allele Identifier: CA185996146

Gene: CCDC26

Linked Data

• dbSNP Id: rs753319506
• gnomAD v3: 8-129559791-G-A
• gnomAD v4: 8-129559791-G-A
• MyVariant Identifiers: chr8:g.130572037G>A (hg19) ; chr8:g.129559791G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559791G>A , CM000670.2:g.129559791G>A	GRCh38
NC_000008.10:g.130572037G>A , CM000670.1:g.130572037G>A	GRCh37
NC_000008.9:g.130641219G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79101C>T
NR_130918.1:n.137+15091C>T
NR_130919.1:n.137+15091C>T
NR_130920.1:n.137+15091C>T