Canonical Allele Identifier: CA652614940
Gene: CCDC26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601232A>C , CM000670.2:g.129601232A>C GRCh38
NC_000008.10:g.130613478A>C , CM000670.1:g.130613478A>C GRCh37
NC_000008.9:g.130682660A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78696T>G