ClinGen Allele Registry
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Canonical Allele Identifier:
CA11489104
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.186841671G>A
GRCh37
chr3:g.186559460G>A
Linked Data - Sequence & Population
gnomAD v2:
3:186559460 G / A
gnomAD v3:
3:186841671 G / A
gnomAD v4:
chr3-186841671-G-A
Joint Max Group AF
0.07862904 (NFE)
Genomes Max Group AF
0.07862904 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17300539
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186841671G>A , CM000665.2:g.186841671G>A
GRCh38
NC_000003.11:g.186559460G>A , CM000665.1:g.186559460G>A
GRCh37
NC_000003.10:g.188042154G>A
NCBI36
NG_021140.1:g.3998G>A
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