Canonical Allele Identifier: CA1119164187
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030288219
gnomAD v3: 8-129601343-T-C
gnomAD v4: 8-129601343-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601343T>C , CM000670.2:g.129601343T>C GRCh38
NC_000008.10:g.130613589T>C , CM000670.1:g.130613589T>C GRCh37
NC_000008.9:g.130682771T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78585A>G
Search 100 bp 5'
Search 100 bp 3'