Allele Registry

Canonical Allele Identifier: CA11116365

Gene: LINC01122 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.59055456T>C

GRCh37 chr2:g.59282591T>C

Linked Data - Sequence & Population

gnomAD v2:

2:59282591 T / C

gnomAD v3:

2:59055456 T / C

gnomAD v4:

chr2-59055456-T-C

Joint Max Group AF 0.81293147 (AFR)

Genomes Max Group AF 0.81293147 (AFR)

Linked Data - NCBI & NCI

dbSNP:

991964

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.59055456T>C , CM000664.2:g.59055456T>C	GRCh38
NC_000002.11:g.59282591T>C , CM000664.1:g.59282591T>C	GRCh37
NC_000002.10:g.59136095T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033873.1:n.1273-3105T>C

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