Canonical Allele Identifier: CA1819332004
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1820172548

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465587G>A , CM000670.2:g.129465587G>A GRCh38
NC_000008.10:g.130477833G>A , CM000670.1:g.130477833G>A GRCh37
NC_000008.9:g.130547015G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15056C>T
NR_130918.1:n.138-95210C>T
NR_130919.1:n.138-65903C>T
NR_130920.1:n.138-65903C>T