ClinGen Allele Registry
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Canonical Allele Identifier:
CA97869569
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.58438966A>G
GRCh37
chr4:g.59305132A>G
Linked Data - Sequence & Population
gnomAD v2:
4:59305132 A / G
gnomAD v3:
4:58438966 A / G
gnomAD v4:
chr4-58438966-A-G
Joint Max Group AF
0.5460565 (AFR)
Genomes Max Group AF
0.5460565 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1869463
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.58438966A>G , CM000666.2:g.58438966A>G
GRCh38
NC_000004.11:g.59305132A>G , CM000666.1:g.59305132A>G
GRCh37
NC_000004.10:g.58999889A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'