Canonical Allele Identifier: CA847371756
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1402210032
MyVariant Identifiers: chr8:g.130572294_130572295insAC (hg19) chr8:g.129560048_129560049insAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560049_129560050insCA , CM000670.2:g.129560049_129560050insCA GRCh38
NC_000008.10:g.130572295_130572296insCA , CM000670.1:g.130572295_130572296insCA GRCh37
NC_000008.9:g.130641477_130641478insCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79359_313-79358insGT
NR_130918.1:n.137+14833_137+14834insGT
NR_130919.1:n.137+14833_137+14834insGT
NR_130920.1:n.137+14833_137+14834insGT
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