Canonical Allele Identifier: CA847373318
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1353494220
gnomAD v3: 8-129465547-C-CA
gnomAD v4: 8-129465547-C-CA
MyVariant Identifiers: chr8:g.130477793_130477794insA (hg19) chr8:g.129465547_129465548insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465553dup , CM000670.2:g.129465553dup GRCh38
NC_000008.10:g.130477799dup , CM000670.1:g.130477799dup GRCh37
NC_000008.9:g.130546981dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15095dup
NR_130918.1:n.138-95171dup
NR_130919.1:n.138-65864dup
NR_130920.1:n.138-65864dup
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