Canonical Allele Identifier: CA1819397384
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560062T= , CM000670.2:g.129560062T= GRCh38
NC_000008.10:g.130572308T= , CM000670.1:g.130572308T= GRCh37
NC_000008.9:g.130641490T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79372A=
NR_130918.1:n.137+14820A=
NR_130919.1:n.137+14820A=
NR_130920.1:n.137+14820A=