Canonical Allele Identifier: CA1119153688
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030944815
gnomAD v3: 8-129633316-G-T
gnomAD v4: 8-129633316-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633316G>T , CM000670.2:g.129633316G>T GRCh38
NC_000008.10:g.130645562G>T , CM000670.1:g.130645562G>T GRCh37
NC_000008.9:g.130714744G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46612C>A
Search 100 bp 5'
Search 100 bp 3'