Canonical Allele Identifier: CA847373227
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1194446398
MyVariant Identifiers: chr8:g.130477606C>T (hg19) chr8:g.129465360C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465360C>T , CM000670.2:g.129465360C>T GRCh38
NC_000008.10:g.130477606C>T , CM000670.1:g.130477606C>T GRCh37
NC_000008.9:g.130546788C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15283G>A
NR_130918.1:n.138-94983G>A
NR_130919.1:n.138-65676G>A
NR_130920.1:n.138-65676G>A
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