Canonical Allele Identifier: CA186000941
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs562891732
gnomAD v3: 8-129601287-G-T
gnomAD v4: 8-129601287-G-T
MyVariant Identifiers: chr8:g.130613533G>T (hg19) chr8:g.129601287G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601287G>T , CM000670.2:g.129601287G>T GRCh38
NC_000008.10:g.130613533G>T , CM000670.1:g.130613533G>T GRCh37
NC_000008.9:g.130682715G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78641C>A
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Search 100 bp 3'