Allele Registry

Canonical Allele Identifier: CA100141904

Gene: LINC02562 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.75105711A>G

GRCh37 chr4:g.76030921A>G

Linked Data - Sequence & Population

gnomAD v2:

4:76030921 A / G

gnomAD v3:

4:75105711 A / G

gnomAD v4:

chr4-75105711-A-G

Joint Max Group AF 0.43330217 (AFR)

Genomes Max Group AF 0.43330217 (AFR)

Linked Data - NCBI & NCI

dbSNP:

1426063

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.75105711A>G , CM000666.2:g.75105711A>G	GRCh38
NC_000004.11:g.76030921A>G , CM000666.1:g.76030921A>G	GRCh37
NC_000004.10:g.76249945A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938888.1:n.236-4296T>C
XR_938889.1:n.135-4296T>C

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