ClinGen Allele Registry
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Canonical Allele Identifier:
CA92203094
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.10060702G>A
GRCh37
chr4:g.10062326G>A
Linked Data - Sequence & Population
gnomAD v2:
4:10062326 G / A
gnomAD v3:
4:10060702 G / A
gnomAD v4:
chr4-10060702-G-A
Joint Max Group AF
0.77742224 (NFE)
Genomes Max Group AF
0.77742224 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6834555
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.10060702G>A , CM000666.2:g.10060702G>A
GRCh38
NC_000004.11:g.10062326G>A , CM000666.1:g.10062326G>A
GRCh37
NC_000004.10:g.9671424G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'