Canonical Allele Identifier: CA847373328
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1403708851
gnomAD v3: 8-129465555-CCTGGGTTTTTCTAAATCATTACGTCTAA-C
gnomAD v4: 8-129465555-CCTGGGTTTTTCTAAATCATTACGTCTAA-C
MyVariant Identifiers: chr8:g.130477802_130477829del (hg19) chr8:g.129465556_129465583del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465563_129465590del , CM000670.2:g.129465563_129465590del GRCh38
NC_000008.10:g.130477809_130477836del , CM000670.1:g.130477809_130477836del GRCh37
NC_000008.9:g.130546991_130547018del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15060_360+15087del
NR_130918.1:n.138-95206_138-95179del
NR_130919.1:n.138-65899_138-65872del
NR_130920.1:n.138-65899_138-65872del
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