Canonical Allele Identifier: CA1119137313
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1820173476

Genomic Alleles

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

Transcript Alleles

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