Canonical Allele Identifier: CA1819332053
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465630C= , CM000670.2:g.129465630C= GRCh38
NC_000008.10:g.130477876C= , CM000670.1:g.130477876C= GRCh37
NC_000008.9:g.130547058C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.360+15013G=
NR_130918.1:n.138-95253G=
NR_130919.1:n.138-65946G=
NR_130920.1:n.138-65946G=