Allele Registry

Canonical Allele Identifier: CA11547671

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr3:g.7941140T>C

GRCh37 chr3:g.7982827T>C

Linked Data - Sequence & Population

gnomAD v2:

3:7982827 T / C

gnomAD v3:

3:7941140 T / C

gnomAD v4:

chr3-7941140-T-C

Joint Max Group AF 0.43771154 (EAS)

Genomes Max Group AF 0.43771154 (EAS)

Linked Data - NCBI & NCI

dbSNP:

4591494

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.7941140T>C , CM000665.2:g.7941140T>C	GRCh38
NC_000003.11:g.7982827T>C , CM000665.1:g.7982827T>C	GRCh37
NC_000003.10:g.7957827T>C	NCBI36

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