ClinGen Allele Registry
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Canonical Allele Identifier:
CA87625126
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765346A>T
GRCh37
chr3:g.169483134A>T
Linked Data - Sequence & Population
gnomAD v3:
3:169765346 A / T
gnomAD v4:
chr3-169765346-A-T
Joint Max Group AF
0.0000729 (SAS)
Genomes Max Group AF
0.0000729 (SAS)
Linked Data - NCBI & NCI
dbSNP:
546654815
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765346A>T , CM000665.2:g.169765346A>T
GRCh38
NC_000003.11:g.169483134A>T , CM000665.1:g.169483134A>T
GRCh37
NC_000003.10:g.170965828A>T
NCBI36
NG_016363.1:g.4715T>A , LRG_347:g.4715T>A
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