Canonical Allele Identifier: CA585157829

Gene: CCDC26

Linked Data

• dbSNP Id: rs1232181320
• gnomAD v2: 8-130572177-A-G
• gnomAD v3: 8-129559931-A-G
• gnomAD v4: 8-129559931-A-G
• COSMIC: COSN22162713
• MyVariant Identifiers: chr8:g.130572177A>G (hg19) ; chr8:g.129559931A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559931A>G , CM000670.2:g.129559931A>G	GRCh38
NC_000008.10:g.130572177A>G , CM000670.1:g.130572177A>G	GRCh37
NC_000008.9:g.130641359A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79241T>C
NR_130918.1:n.137+14951T>C
NR_130919.1:n.137+14951T>C
NR_130920.1:n.137+14951T>C