ClinGen Allele Registry
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Canonical Allele Identifier:
CA11380973
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.143264057A>G
GRCh37
chr3:g.142982899A>G
Linked Data - Sequence & Population
gnomAD v2:
3:142982899 A / G
gnomAD v3:
3:143264057 A / G
gnomAD v4:
chr3-143264057-A-G
Joint Max Group AF
0.53215324 (NFE)
Genomes Max Group AF
0.53215324 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9810857
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.143264057A>G , CM000665.2:g.143264057A>G
GRCh38
NC_000003.11:g.142982899A>G , CM000665.1:g.142982899A>G
GRCh37
NC_000003.10:g.144465589A>G
NCBI36
NG_017077.1:g.589475T>C
NG_017077.2:g.589475T>C
Search 100 bp 5'
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