ClinGen Allele Registry
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Canonical Allele Identifier:
CA847392989
Gene: CCDC26
HGNC
NCBI
Linked Data
dbSNP Id:
rs1360294226
gnomAD v3:
8-129601412-A-C
gnomAD v4:
8-129601412-A-C
MyVariant Identifiers:
chr8:g.130613658A>C (hg19)
chr8:g.129601412A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.129601412A>C , CM000670.2:g.129601412A>C
GRCh38
NC_000008.10:g.130613658A>C , CM000670.1:g.130613658A>C
GRCh37
NC_000008.9:g.130682840A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_130917.1:n.312+78516T>G
Search 100 bp 5'
Search 100 bp 3'