Canonical Allele Identifier: CA11515839
Gene:
MyVariant.info:
GRCh38 chr3:g.169764347G>A
GRCh37 chr3:g.169482135G>A
gnomAD v2:
3:169482135 G / A
gnomAD v3:
3:169764347 G / A
gnomAD v4:
chr3-169764347-G-A
Joint Max Group AF 0.01596982 (MID)
Genomes Max Group AF 0.01498997 (NFE)
ClinVar RCV:
RCV001550719
ClinVar Variation:
1190126
dbSNP:
35073794
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764347G>A , CM000665.2:g.169764347G>A GRCh38
NC_000003.11:g.169482135G>A , CM000665.1:g.169482135G>A GRCh37
NC_000003.10:g.170964829G>A NCBI36
NG_016363.1:g.5714C>T , LRG_347:g.5714C>T
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