Canonical Allele Identifier: CA185985532
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs893135014
gnomAD v3: 8-129465529-CATCA-C
gnomAD v4: 8-129465529-CATCA-C
MyVariant Identifiers: chr8:g.130477776_130477779del (hg19) chr8:g.129465530_129465533del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465536_129465539del , CM000670.2:g.129465536_129465539del GRCh38
NC_000008.10:g.130477782_130477785del , CM000670.1:g.130477782_130477785del GRCh37
NC_000008.9:g.130546964_130546967del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15110_360+15113del
NR_130918.1:n.138-95156_138-95153del
NR_130919.1:n.138-65849_138-65846del
NR_130920.1:n.138-65849_138-65846del
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