Canonical Allele Identifier: CA847393078
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1360381434
gnomAD v3: 8-129601533-TCTAGTC-T
gnomAD v4: 8-129601533-TCTAGTC-T
MyVariant Identifiers: chr8:g.130613780_130613785del (hg19) chr8:g.129601534_129601539del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601539_129601544del , CM000670.2:g.129601539_129601544del GRCh38
NC_000008.10:g.130613785_130613790del , CM000670.1:g.130613785_130613790del GRCh37
NC_000008.9:g.130682967_130682972del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78389_312+78394del
Search 100 bp 5'
Search 100 bp 3'