ClinGen Allele Registry
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Canonical Allele Identifier:
CA11725799
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.68671757A>G
GRCh37
chr4:g.69537475A>G
Linked Data - Sequence & Population
gnomAD v2:
4:69537475 A / G
gnomAD v3:
4:68671757 A / G
gnomAD v4:
chr4-68671757-A-G
Joint Max Group AF
0.60342953 (AFR)
Genomes Max Group AF
0.60342953 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9994887
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.68671757A>G , CM000666.2:g.68671757A>G
GRCh38
NC_000004.11:g.69537475A>G , CM000666.1:g.69537475A>G
GRCh37
NC_000004.10:g.69220070A>G
NCBI36
NG_052676.1:g.4020T>C
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