Canonical Allele Identifier: CA186000967
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs968846198
MyVariant Identifiers: chr8:g.129601488A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601488A>C , CM000670.2:g.129601488A>C GRCh38
NC_000008.10:g.130613734A>C , CM000670.1:g.130613734A>C GRCh37
NC_000008.9:g.130682916A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78440T>G
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