Canonical Allele Identifier: CA185985518
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs185716159
gnomAD v2: 8-130477611-A-C
gnomAD v3: 8-129465365-A-C
gnomAD v4: 8-129465365-A-C
MyVariant Identifiers: chr8:g.130477611A>C (hg19) chr8:g.129465365A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465365A>C , CM000670.2:g.129465365A>C GRCh38
NC_000008.10:g.130477611A>C , CM000670.1:g.130477611A>C GRCh37
NC_000008.9:g.130546793A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15278T>G
NR_130918.1:n.138-94988T>G
NR_130919.1:n.138-65681T>G
NR_130920.1:n.138-65681T>G
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