Allele Registry

Canonical Allele Identifier: CA11618449

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr3:g.41096181A>G

GRCh37 chr3:g.41137672A>G

Linked Data - Sequence & Population

gnomAD v2:

3:41137672 A / G

gnomAD v3:

3:41096181 A / G

gnomAD v4:

chr3-41096181-A-G

Joint Max Group AF 0.77246687 (AFR)

Genomes Max Group AF 0.77246687 (AFR)

Linked Data - NCBI & NCI

dbSNP:

87938

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41096181A>G , CM000665.2:g.41096181A>G	GRCh38
NC_000003.11:g.41137672A>G , CM000665.1:g.41137672A>G	GRCh37
NC_000003.10:g.41112676A>G	NCBI36

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