Canonical Allele Identifier: CA847411990
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1314623800
MyVariant Identifiers: chr8:g.130645555A>C (hg19) chr8:g.129633309A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633309A>C , CM000670.2:g.129633309A>C GRCh38
NC_000008.10:g.130645555A>C , CM000670.1:g.130645555A>C GRCh37
NC_000008.9:g.130714737A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46619T>G
Search 100 bp 5'
Search 100 bp 3'