Canonical Allele Identifier: CA185985521
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs923792683
gnomAD v3: 8-129465404-ACT-A
gnomAD v4: 8-129465404-ACT-A
MyVariant Identifiers: chr8:g.130477651_130477652del (hg19) chr8:g.129465405_129465406del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465409_129465410del , CM000670.2:g.129465409_129465410del GRCh38
NC_000008.10:g.130477655_130477656del , CM000670.1:g.130477655_130477656del GRCh37
NC_000008.9:g.130546837_130546838del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15237_360+15238del
NR_130918.1:n.138-95029_138-95028del
NR_130919.1:n.138-65722_138-65721del
NR_130920.1:n.138-65722_138-65721del
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