Allele Registry

Canonical Allele Identifier: CA15107829

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.65703996G>A

GRCh37 chr1:g.66169679G>A

Linked Data - Sequence & Population

gnomAD v2:

1:66169679 G / A

gnomAD v3:

1:65703996 G / A

gnomAD v4:

chr1-65703996-G-A

Joint Max Group AF 0.61800599 (NFE)

Genomes Max Group AF 0.61803458 (NFE)

Exomes Max Group AF 0.48991068 (NFE)

Linked Data - NCBI & NCI

dbSNP:

12753193

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65703996G>A , CM000663.2:g.65703996G>A	GRCh38
NC_000001.10:g.66169679G>A , CM000663.1:g.66169679G>A	GRCh37
NC_000001.9:g.65942267G>A	NCBI36

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