Canonical Allele Identifier: CA585154788
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1292871066
gnomAD v2: 8-130477782-CAATT-C
gnomAD v3: 8-129465536-CAATT-C
gnomAD v4: 8-129465536-CAATT-C
MyVariant Identifiers: chr8:g.130477783_130477786del (hg19) chr8:g.129465537_129465540del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465538_129465541del , CM000670.2:g.129465538_129465541del GRCh38
NC_000008.10:g.130477784_130477787del , CM000670.1:g.130477784_130477787del GRCh37
NC_000008.9:g.130546966_130546969del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15103_360+15106del
NR_130918.1:n.138-95163_138-95160del
NR_130919.1:n.138-65856_138-65853del
NR_130920.1:n.138-65856_138-65853del
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