ClinGen Allele Registry
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Canonical Allele Identifier:
CA11725803
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.68672462G>A
GRCh37
chr4:g.69538180G>A
Linked Data - Sequence & Population
gnomAD v2:
4:69538180 G / A
gnomAD v3:
4:68672462 G / A
gnomAD v4:
chr4-68672462-G-A
Joint Max Group AF
0.60152607 (AFR)
Genomes Max Group AF
0.60152607 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7696472
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.68672462G>A , CM000666.2:g.68672462G>A
GRCh38
NC_000004.11:g.69538180G>A , CM000666.1:g.69538180G>A
GRCh37
NC_000004.10:g.69220775G>A
NCBI36
NG_052676.1:g.3315C>T
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