ClinGen Allele Registry
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Canonical Allele Identifier:
CA279690671
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr16:g.27366928A>C
Linked Data - Sequence & Population
gnomAD v3:
16:27366928 A / C
gnomAD v4:
chr16-27366928-A-C
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4787956
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.27366928A>C , CM000678.2:g.27366928A>C
GRCh38
NC_000016.9:g.27378249A>C , CM000678.1:g.27378249A>C
GRCh37
NC_000016.8:g.27285750A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'