Canonical Allele Identifier: CA185985531
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs566582197
gnomAD v3: 8-129465522-C-A
gnomAD v4: 8-129465522-C-A
MyVariant Identifiers: chr8:g.130477768C>A (hg19) chr8:g.129465522C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465522C>A , CM000670.2:g.129465522C>A GRCh38
NC_000008.10:g.130477768C>A , CM000670.1:g.130477768C>A GRCh37
NC_000008.9:g.130546950C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15121G>T
NR_130918.1:n.138-95145G>T
NR_130919.1:n.138-65838G>T
NR_130920.1:n.138-65838G>T
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