Canonical Allele Identifier: CA1819397441
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1586474761
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560135C>T , CM000670.2:g.129560135C>T GRCh38
NC_000008.10:g.130572381C>T , CM000670.1:g.130572381C>T GRCh37
NC_000008.9:g.130641563C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79445G>A
NR_130918.1:n.137+14747G>A
NR_130919.1:n.137+14747G>A
NR_130920.1:n.137+14747G>A
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