Allele Registry

Canonical Allele Identifier: CA16490884

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr14:g.57355498G>A

GRCh37 chr14:g.57822216G>A

Linked Data - Sequence & Population

gnomAD v2:

14:57822216 G / A

gnomAD v3:

14:57355498 G / A

gnomAD v4:

chr14-57355498-G-A

Joint Max Group AF 0.76819463 (NFE)

Genomes Max Group AF 0.76818784 (NFE)

Exomes Max Group AF 0.17768 (NFE)

Linked Data - NCBI & NCI

dbSNP:

7144649

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.57355498G>A , CM000676.2:g.57355498G>A	GRCh38
NC_000014.8:g.57822216G>A , CM000676.1:g.57822216G>A	GRCh37
NC_000014.7:g.56891969G>A	NCBI36

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