ClinGen Allele Registry
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Canonical Allele Identifier:
CA32667122
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.171652737A>G
GRCh37
chr1:g.171621877A>G
Linked Data - Sequence & Population
gnomAD v2:
1:171621877 A / G
gnomAD v3:
1:171652737 A / G
gnomAD v4:
chr1-171652737-A-G
Joint Max Group AF
0.04027215 (MID)
Genomes Max Group AF
0.02917489 (NFE)
Exomes Max Group AF
0.03871633 (MID)
Linked Data - NCBI & NCI
dbSNP:
34928744
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.171652737A>G , CM000663.2:g.171652737A>G
GRCh38
NC_000001.10:g.171621877A>G , CM000663.1:g.171621877A>G
GRCh37
NC_000001.9:g.169888500A>G
NCBI36
NG_008859.1:g.4897T>C
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