Allele Registry

Canonical Allele Identifier: CA2696853

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr3:g.169765159G>C

GRCh37 chr3:g.169482947G>C

Linked Data - Sequence & Population

gnomAD v2:

3:169482947 G / C

gnomAD v3:

3:169765159 G / C

gnomAD v4:

chr3-169765159-G-C

Joint Max Group AF 0.00093083 (NFE)

Genomes Max Group AF 0.00079493 (NFE)

Exomes Max Group AF 0.00092866 (NFE)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001561876

RCV001820784

ClinVar Variation:

242267

dbSNP:

540289812

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765159G>C , CM000665.2:g.169765159G>C	GRCh38
NC_000003.11:g.169482947G>C , CM000665.1:g.169482947G>C	GRCh37
NC_000003.10:g.170965641G>C	NCBI36
NG_016363.1:g.4902C>G , LRG_347:g.4902C>G

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