Allele Registry

Canonical Allele Identifier: CA13404971

Gene: LINC02714 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.134756993T>C

GRCh37 chr11:g.134626887T>C

Linked Data - Sequence & Population

gnomAD v2:

11:134626887 T / C

gnomAD v3:

11:134756993 T / C

gnomAD v4:

chr11-134756993-T-C

Joint Max Group AF 0.17494436 (MID)

Genomes Max Group AF 0.15360144 (AMR)

Linked Data - NCBI & NCI

dbSNP:

11223996

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134756993T>C , CM000673.2:g.134756993T>C	GRCh38
NC_000011.9:g.134626887T>C , CM000673.1:g.134626887T>C	GRCh37
NC_000011.8:g.134132097T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_147836.1:n.599-4081T>C

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