Canonical Allele Identifier: CA1119164224
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1743770053
gnomAD v3: 8-129601442-T-G
gnomAD v4: 8-129601442-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601442T>G , CM000670.2:g.129601442T>G GRCh38
NC_000008.10:g.130613688T>G , CM000670.1:g.130613688T>G GRCh37
NC_000008.9:g.130682870T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78486A>C
Search 100 bp 5'
Search 100 bp 3'