Canonical Allele Identifier: CA1819427311
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs930532855
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633432G>T , CM000670.2:g.129633432G>T GRCh38
NC_000008.10:g.130645678G>T , CM000670.1:g.130645678G>T GRCh37
NC_000008.9:g.130714860G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46496C>A
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