Canonical Allele Identifier: CA185985519
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs536250987
gnomAD v3: 8-129465375-T-C
gnomAD v4: 8-129465375-T-C
MyVariant Identifiers: chr8:g.130477621T>C (hg19) chr8:g.129465375T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465375T>C , CM000670.2:g.129465375T>C GRCh38
NC_000008.10:g.130477621T>C , CM000670.1:g.130477621T>C GRCh37
NC_000008.9:g.130546803T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15268A>G
NR_130918.1:n.138-94998A>G
NR_130919.1:n.138-65691A>G
NR_130920.1:n.138-65691A>G
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