Canonical Allele Identifier: CA2782190033
Gene: CCDC26 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560036G>T , CM000670.2:g.129560036G>T GRCh38
NC_000008.10:g.130572282G>T , CM000670.1:g.130572282G>T GRCh37
NC_000008.9:g.130641464G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79346C>A
NR_130918.1:n.137+14846C>A
NR_130919.1:n.137+14846C>A
NR_130920.1:n.137+14846C>A
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