Canonical Allele Identifier: CA186004554
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs868370121
MyVariant Identifiers: chr8:g.130645535G>A (hg19) chr8:g.129633289G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633289G>A , CM000670.2:g.129633289G>A GRCh38
NC_000008.10:g.130645535G>A , CM000670.1:g.130645535G>A GRCh37
NC_000008.9:g.130714717G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46639C>T
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Search 100 bp 3'