Allele Registry

Canonical Allele Identifier: CA229677615

Gene: USP2-AS1 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.119399248G>A

GRCh37 chr11:g.119269958G>A

Linked Data - Sequence & Population

gnomAD v2:

11:119269958 G / A

gnomAD v3:

11:119399248 G / A

gnomAD v4:

chr11-119399248-G-A

Joint Max Group AF 0.00346899 (NFE)

Genomes Max Group AF 0.00346899 (NFE)

Linked Data - NCBI & NCI

dbSNP:

139137459

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119399248G>A , CM000673.2:g.119399248G>A	GRCh38
NC_000011.9:g.119269958G>A , CM000673.1:g.119269958G>A	GRCh37
NC_000011.8:g.118775168G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034160.1:n.305+4094G>A

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