Canonical Allele Identifier: CA1119164179
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030288112
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601338A>G , CM000670.2:g.129601338A>G GRCh38
NC_000008.10:g.130613584A>G , CM000670.1:g.130613584A>G GRCh37
NC_000008.9:g.130682766A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78590T>C
Search 100 bp 5'
Search 100 bp 3'