Canonical Allele Identifier: CA87625098
Gene:

Linked Data

ClinVar Variation Id: 2628804
ClinVar RCV Id: RCV003399611
dbSNP Id: rs889076835
gnomAD v3: 3-169765293-G-A
gnomAD v4: 3-169765293-G-A
MyVariant Identifiers: chr3:g.169483081G>A (hg19) chr3:g.169765293G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765293G>A , CM000665.2:g.169765293G>A GRCh38
NC_000003.11:g.169483081G>A , CM000665.1:g.169483081G>A GRCh37
NC_000003.10:g.170965775G>A NCBI36
NG_016363.1:g.4768C>T , LRG_347:g.4768C>T
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