Allele Registry

Canonical Allele Identifier: CA264594501

Gene: LINC02301 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr14:g.82739693A>G

GRCh37 chr14:g.83206037A>G

Linked Data - Sequence & Population

gnomAD v2:

14:83206037 A / G

gnomAD v3:

14:82739693 A / G

gnomAD v4:

chr14-82739693-A-G

Joint Max Group AF 0.32599096 (AMR)

Genomes Max Group AF 0.32599096 (AMR)

Linked Data - NCBI & NCI

dbSNP:

1242541

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.82739693A>G , CM000676.2:g.82739693A>G	GRCh38
NC_000014.8:g.83206037A>G , CM000676.1:g.83206037A>G	GRCh37
NC_000014.7:g.82275790A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_944088.1:n.362-1006A>G

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