ClinGen Allele Registry
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Canonical Allele Identifier:
CA283066451
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.65883303A>G
GRCh37
chr16:g.65917206A>G
Linked Data - Sequence & Population
gnomAD v2:
16:65917206 A / G
gnomAD v3:
16:65883303 A / G
gnomAD v4:
chr16-65883303-A-G
Joint Max Group AF
0.1931792 (AFR)
Genomes Max Group AF
0.1931792 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7188225
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.65883303A>G , CM000678.2:g.65883303A>G
GRCh38
NC_000016.9:g.65917206A>G , CM000678.1:g.65917206A>G
GRCh37
NC_000016.8:g.64474707A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'