Canonical Allele Identifier: CA185985537
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1003429328
MyVariant Identifiers: chr8:g.130477843A>G (hg19) chr8:g.129465597A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465597A>G , CM000670.2:g.129465597A>G GRCh38
NC_000008.10:g.130477843A>G , CM000670.1:g.130477843A>G GRCh37
NC_000008.9:g.130547025A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.360+15046T>C
NR_130918.1:n.138-95220T>C
NR_130919.1:n.138-65913T>C
NR_130920.1:n.138-65913T>C
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