Canonical Allele Identifier: CA1819332009
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1820172593

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465595T>G , CM000670.2:g.129465595T>G GRCh38
NC_000008.10:g.130477841T>G , CM000670.1:g.130477841T>G GRCh37
NC_000008.9:g.130547023T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15048A>C
NR_130918.1:n.138-95218A>C
NR_130919.1:n.138-65911A>C
NR_130920.1:n.138-65911A>C