Canonical Allele Identifier: CA185996181
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs978201114
gnomAD v3: 8-129560089-T-G
gnomAD v4: 8-129560089-T-G
MyVariant Identifiers: chr8:g.130572335T>G (hg19) chr8:g.129560089T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560089T>G , CM000670.2:g.129560089T>G GRCh38
NC_000008.10:g.130572335T>G , CM000670.1:g.130572335T>G GRCh37
NC_000008.9:g.130641517T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79399A>C
NR_130918.1:n.137+14793A>C
NR_130919.1:n.137+14793A>C
NR_130920.1:n.137+14793A>C
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