ClinGen Allele Registry
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Canonical Allele Identifier:
CA14247912
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56951227A>G
GRCh37
chr16:g.56985139A>G
Linked Data - Sequence & Population
gnomAD v2:
16:56985139 A / G
gnomAD v3:
16:56951227 A / G
gnomAD v4:
chr16-56951227-A-G
Joint Max Group AF
0.74070242 (EAS)
Genomes Max Group AF
0.74070242 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9989419
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56951227A>G , CM000678.2:g.56951227A>G
GRCh38
NC_000016.9:g.56985139A>G , CM000678.1:g.56985139A>G
GRCh37
NC_000016.8:g.55542640A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'