Canonical Allele Identifier: CA1819331743
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1308609373

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465409C>G , CM000670.2:g.129465409C>G GRCh38
NC_000008.10:g.130477655C>G , CM000670.1:g.130477655C>G GRCh37
NC_000008.9:g.130546837C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15234G>C
NR_130918.1:n.138-95032G>C
NR_130919.1:n.138-65725G>C
NR_130920.1:n.138-65725G>C