Canonical Allele Identifier: CA1819414250
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030290840

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601492G>T , CM000670.2:g.129601492G>T GRCh38
NC_000008.10:g.130613738G>T , CM000670.1:g.130613738G>T GRCh37
NC_000008.9:g.130682920G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78436C>A