Canonical Allele Identifier: CA585154789
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1442993506
gnomAD v2: 8-130477818-C-A
gnomAD v3: 8-129465572-C-A
gnomAD v4: 8-129465572-C-A
MyVariant Identifiers: chr8:g.130477818C>A (hg19) chr8:g.129465572C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465572C>A , CM000670.2:g.129465572C>A GRCh38
NC_000008.10:g.130477818C>A , CM000670.1:g.130477818C>A GRCh37
NC_000008.9:g.130547000C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15071G>T
NR_130918.1:n.138-95195G>T
NR_130919.1:n.138-65888G>T
NR_130920.1:n.138-65888G>T
Search 100 bp 5'
Search 100 bp 3'