Canonical Allele Identifier: CA186004558
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1023239538
MyVariant Identifiers: chr8:g.130645554G>A (hg19) chr8:g.129633308G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633308G>A , CM000670.2:g.129633308G>A GRCh38
NC_000008.10:g.130645554G>A , CM000670.1:g.130645554G>A GRCh37
NC_000008.9:g.130714736G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46620C>T
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