Canonical Allele Identifier: CA11427621
Gene:
MyVariant.info:
GRCh38 chr3:g.169764547T>C
GRCh37 chr3:g.169482335T>C
gnomAD v2:
3:169482335 T / C
gnomAD v3:
3:169764547 T / C
gnomAD v4:
chr3-169764547-T-C
Joint Max Group AF 0.59866302 (EAS)
Genomes Max Group AF 0.54498008 (EAS)
Exomes Max Group AF 0.60483768 (EAS)
ClinVar Allele:
433966
ClinVar RCV:
RCV000508369
RCV001518928
ClinVar Variation:
440330
dbSNP:
2293607
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764547T>C , CM000665.2:g.169764547T>C GRCh38
NC_000003.11:g.169482335T>C , CM000665.1:g.169482335T>C GRCh37
NC_000003.10:g.170965029T>C NCBI36
NG_016363.1:g.5514A>G , LRG_347:g.5514A>G
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