Canonical Allele Identifier: CA1819414218
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030289714

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601438A>G , CM000670.2:g.129601438A>G GRCh38
NC_000008.10:g.130613684A>G , CM000670.1:g.130613684A>G GRCh37
NC_000008.9:g.130682866A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78490T>C