Canonical Allele Identifier: CA1819414291
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030292470

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601576T>G , CM000670.2:g.129601576T>G GRCh38
NC_000008.10:g.130613822T>G , CM000670.1:g.130613822T>G GRCh37
NC_000008.9:g.130683004T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78352A>C