Canonical Allele Identifier: CA11515839
Gene:

Linked Data

ClinVar Variation Id: 1190126
ClinVar RCV Id: RCV001550719
dbSNP Id: rs35073794
gnomAD v2: 3-169482135-G-A
gnomAD v3: 3-169764347-G-A
gnomAD v4: 3-169764347-G-A
MyVariant Identifiers: chr3:g.169482135G>A (hg19) chr3:g.169764347G>A (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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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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