Allele Registry

Canonical Allele Identifier: CA16094106

Gene: LINC01320 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.34687783G>A

GRCh37 chr2:g.34912850G>A

Linked Data - Sequence & Population

gnomAD v2:

2:34912850 G / A

gnomAD v3:

2:34687783 G / A

gnomAD v4:

chr2-34687783-G-A

Joint Max Group AF 0.73200117 (EAS)

Genomes Max Group AF 0.73200117 (EAS)

Linked Data - NCBI & NCI

dbSNP:

11683103

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.34687783G>A , CM000664.2:g.34687783G>A	GRCh38
NC_000002.11:g.34912850G>A , CM000664.1:g.34912850G>A	GRCh37
NC_000002.10:g.34766354G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126404.1:n.371+9856G>A

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