ClinGen Allele Registry
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Canonical Allele Identifier:
CA11725802
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.68672197T>C
GRCh37
chr4:g.69537915T>C
Linked Data - Sequence & Population
gnomAD v2:
4:69537915 T / C
gnomAD v3:
4:68672197 T / C
gnomAD v4:
chr4-68672197-T-C
Joint Max Group AF
0.60197144 (AFR)
Genomes Max Group AF
0.60197144 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7686914
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.68672197T>C , CM000666.2:g.68672197T>C
GRCh38
NC_000004.11:g.69537915T>C , CM000666.1:g.69537915T>C
GRCh37
NC_000004.10:g.69220510T>C
NCBI36
NG_052676.1:g.3580A>G
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