ClinGen Allele Registry
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Canonical Allele Identifier:
CA89835409
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.185904041G>A
GRCh37
chr3:g.185621829G>A
Linked Data - Sequence & Population
gnomAD v2:
3:185621829 G / A
gnomAD v3:
3:185904041 G / A
gnomAD v4:
chr3-185904041-G-A
Joint Max Group AF
0.76814782 (SAS)
Genomes Max Group AF
0.76814782 (SAS)
Linked Data - NCBI & NCI
dbSNP:
6444087
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.185904041G>A , CM000665.2:g.185904041G>A
GRCh38
NC_000003.11:g.185621829G>A , CM000665.1:g.185621829G>A
GRCh37
NC_000003.10:g.187104523G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'