Canonical Allele Identifier: CA1119153743
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030948643
gnomAD v3: 8-129633535-T-C
gnomAD v4: 8-129633535-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633535T>C , CM000670.2:g.129633535T>C GRCh38
NC_000008.10:g.130645781T>C , CM000670.1:g.130645781T>C GRCh37
NC_000008.9:g.130714963T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46393A>G
Search 100 bp 5'
Search 100 bp 3'