Canonical Allele Identifier: CA847393055
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1285061497
gnomAD v3: 8-129601492-G-GT
gnomAD v4: 8-129601492-G-GT
MyVariant Identifiers: chr8:g.130613738_130613739insT (hg19) chr8:g.129601492_129601493insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601498dup , CM000670.2:g.129601498dup GRCh38
NC_000008.10:g.130613744dup , CM000670.1:g.130613744dup GRCh37
NC_000008.9:g.130682926dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78435dup
Search 100 bp 5'
Search 100 bp 3'