Canonical Allele Identifier: CA185996148
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs576433648
gnomAD v3: 8-129559813-C-T
gnomAD v4: 8-129559813-C-T
MyVariant Identifiers: chr8:g.130572059C>T (hg19) chr8:g.129559813C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129559813C>T , CM000670.2:g.129559813C>T GRCh38
NC_000008.10:g.130572059C>T , CM000670.1:g.130572059C>T GRCh37
NC_000008.9:g.130641241C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79123G>A
NR_130918.1:n.137+15069G>A
NR_130919.1:n.137+15069G>A
NR_130920.1:n.137+15069G>A
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