Canonical Allele Identifier: CA2718196079
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2129766219
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465439C>T , CM000670.2:g.129465439C>T GRCh38
NC_000008.10:g.130477685C>T , CM000670.1:g.130477685C>T GRCh37
NC_000008.9:g.130546867C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15204G>A
NR_130918.1:n.138-95062G>A
NR_130919.1:n.138-65755G>A
NR_130920.1:n.138-65755G>A
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