Canonical Allele Identifier: CA1819331848
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1820171374

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465516A>C , CM000670.2:g.129465516A>C GRCh38
NC_000008.10:g.130477762A>C , CM000670.1:g.130477762A>C GRCh37
NC_000008.9:g.130546944A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15127T>G
NR_130918.1:n.138-95139T>G
NR_130919.1:n.138-65832T>G
NR_130920.1:n.138-65832T>G