Canonical Allele Identifier: CA1819414119
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030284242
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601216G>C , CM000670.2:g.129601216G>C GRCh38
NC_000008.10:g.130613462G>C , CM000670.1:g.130613462G>C GRCh37
NC_000008.9:g.130682644G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78712C>G
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Search 100 bp 3'