Canonical Allele Identifier: CA186000946
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1020118885
gnomAD v3: 8-129601363-C-G
gnomAD v4: 8-129601363-C-G
MyVariant Identifiers: chr8:g.130613609C>G (hg19) chr8:g.129601363C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601363C>G , CM000670.2:g.129601363C>G GRCh38
NC_000008.10:g.130613609C>G , CM000670.1:g.130613609C>G GRCh37
NC_000008.9:g.130682791C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78565G>C
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