Canonical Allele Identifier: CA11521805
Gene:
MyVariant.info:
GRCh38 chr3:g.30694445G>A
GRCh37 chr3:g.30735937G>A
gnomAD v2:
3:30735937 G / A
gnomAD v3:
3:30694445 G / A
gnomAD v4:
chr3-30694445-G-A
Joint Max Group AF 0.31242517 (NFE)
Genomes Max Group AF 0.31242517 (NFE)
ClinVar RCV:
RCV001522970
ClinVar Variation:
1170531
dbSNP:
744751
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30694445G>A , CM000665.2:g.30694445G>A GRCh38
NC_000003.11:g.30735937G>A , CM000665.1:g.30735937G>A GRCh37
NC_000003.10:g.30710941G>A NCBI36
NG_007490.1:g.92944G>A , LRG_779:g.92944G>A
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