Canonical Allele Identifier: CA12740299
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs6987588
gnomAD v2: 8-130572304-C-T
gnomAD v3: 8-129560058-C-T
gnomAD v4: 8-129560058-C-T
MyVariant Identifiers: chr8:g.130572304C>T (hg19) chr8:g.129560058C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560058C>T , CM000670.2:g.129560058C>T GRCh38
NC_000008.10:g.130572304C>T , CM000670.1:g.130572304C>T GRCh37
NC_000008.9:g.130641486C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79368G>A
NR_130918.1:n.137+14824G>A
NR_130919.1:n.137+14824G>A
NR_130920.1:n.137+14824G>A
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