Canonical Allele Identifier: CA185985525
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1035489398
MyVariant Identifiers: chr8:g.130477696A>G (hg19) chr8:g.129465450A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465450A>G , CM000670.2:g.129465450A>G GRCh38
NC_000008.10:g.130477696A>G , CM000670.1:g.130477696A>G GRCh37
NC_000008.9:g.130546878A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15193T>C
NR_130918.1:n.138-95073T>C
NR_130919.1:n.138-65766T>C
NR_130920.1:n.138-65766T>C
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