Canonical Allele Identifier: CA186004557
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs914195702
MyVariant Identifiers: chr8:g.130645550G>C (hg19) chr8:g.129633304G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633304G>C , CM000670.2:g.129633304G>C GRCh38
NC_000008.10:g.130645550G>C , CM000670.1:g.130645550G>C GRCh37
NC_000008.9:g.130714732G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46624C>G
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