Canonical Allele Identifier: CA1119164213
Gene: CCDC26 HGNC NCBI

Linked Data

gnomAD v3: 8-129601371-A-T
gnomAD v4: 8-129601371-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601371A>T , CM000670.2:g.129601371A>T GRCh38
NC_000008.10:g.130613617A>T , CM000670.1:g.130613617A>T GRCh37
NC_000008.9:g.130682799A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78557T>A
Search 100 bp 5'
Search 100 bp 3'