Canonical Allele Identifier: CA1819331936
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs984859197
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465547C>A , CM000670.2:g.129465547C>A GRCh38
NC_000008.10:g.130477793C>A , CM000670.1:g.130477793C>A GRCh37
NC_000008.9:g.130546975C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15096G>T
NR_130918.1:n.138-95170G>T
NR_130919.1:n.138-65863G>T
NR_130920.1:n.138-65863G>T
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