Canonical Allele Identifier: CA185996197
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs192846798
gnomAD v2: 8-130572443-G-A
gnomAD v3: 8-129560197-G-A
gnomAD v4: 8-129560197-G-A
MyVariant Identifiers: chr8:g.130572443G>A (hg19) chr8:g.129560197G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560197G>A , CM000670.2:g.129560197G>A GRCh38
NC_000008.10:g.130572443G>A , CM000670.1:g.130572443G>A GRCh37
NC_000008.9:g.130641625G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79507C>T
NR_130918.1:n.137+14685C>T
NR_130919.1:n.137+14685C>T
NR_130920.1:n.137+14685C>T
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