Allele Registry

Canonical Allele Identifier: CA53081665

Gene: LINC01104 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.100219272A>G

GRCh37 chr2:g.100835734A>G

Linked Data - Sequence & Population

gnomAD v2:

2:100835734 A / G

gnomAD v3:

2:100219272 A / G

gnomAD v4:

chr2-100219272-A-G

Joint Max Group AF 0.58341346 (EAS)

Genomes Max Group AF 0.58341346 (EAS)

Linked Data - NCBI & NCI

dbSNP:

10865035

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100219272A>G , CM000664.2:g.100219272A>G	GRCh38
NC_000002.11:g.100835734A>G , CM000664.1:g.100835734A>G	GRCh37
NC_000002.10:g.100202166A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_103730.1:n.567+10452A>G

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