Canonical Allele Identifier: CA2718241124
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2130045507

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601362A>C , CM000670.2:g.129601362A>C GRCh38
NC_000008.10:g.130613608A>C , CM000670.1:g.130613608A>C GRCh37
NC_000008.9:g.130682790A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78566T>G