Canonical Allele Identifier: CA652614964
Gene: CCDC26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601527T>C , CM000670.2:g.129601527T>C GRCh38
NC_000008.10:g.130613773T>C , CM000670.1:g.130613773T>C GRCh37
NC_000008.9:g.130682955T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78401A>G