Canonical Allele Identifier: CA585155596
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1946627

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601247G>T , CM000670.2:g.129601247G>T GRCh38
NC_000008.10:g.130613493G>T , CM000670.1:g.130613493G>T GRCh37
NC_000008.9:g.130682675G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78681C>A