Canonical Allele Identifier: CA847373312
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1288779915
gnomAD v3: 8-129465543-A-C
gnomAD v4: 8-129465543-A-C
MyVariant Identifiers: chr8:g.130477789A>C (hg19) chr8:g.129465543A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465543A>C , CM000670.2:g.129465543A>C GRCh38
NC_000008.10:g.130477789A>C , CM000670.1:g.130477789A>C GRCh37
NC_000008.9:g.130546971A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15100T>G
NR_130918.1:n.138-95166T>G
NR_130919.1:n.138-65859T>G
NR_130920.1:n.138-65859T>G
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