ClinGen Allele Registry
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Canonical Allele Identifier:
CA186000927
Gene: CCDC26
HGNC
NCBI
Linked Data
dbSNP Id:
rs972295762
gnomAD v2:
8-130613428-T-A
gnomAD v3:
8-129601182-T-A
gnomAD v4:
8-129601182-T-A
MyVariant Identifiers:
chr8:g.130613428T>A (hg19)
chr8:g.129601182T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.129601182T>A , CM000670.2:g.129601182T>A
GRCh38
NC_000008.10:g.130613428T>A , CM000670.1:g.130613428T>A
GRCh37
NC_000008.9:g.130682610T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_130917.1:n.312+78746A>T
Search 100 bp 5'
Search 100 bp 3'