Canonical Allele Identifier: CA1819331710
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1820170358
gnomAD v3: 8-129465388-G-T
gnomAD v4: 8-129465388-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465388G>T , CM000670.2:g.129465388G>T GRCh38
NC_000008.10:g.130477634G>T , CM000670.1:g.130477634G>T GRCh37
NC_000008.9:g.130546816G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15255C>A
NR_130918.1:n.138-95011C>A
NR_130919.1:n.138-65704C>A
NR_130920.1:n.138-65704C>A
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