Canonical Allele Identifier: CA847412179
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1440404619
MyVariant Identifiers: chr8:g.130645791C>T (hg19) chr8:g.129633545C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633545C>T , CM000670.2:g.129633545C>T GRCh38
NC_000008.10:g.130645791C>T , CM000670.1:g.130645791C>T GRCh37
NC_000008.9:g.130714973C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46383G>A
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