Allele Registry

Canonical Allele Identifier: CA16358946

Gene: LINC01239 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.22770887A>G

GRCh37 chr9:g.22770886A>G

Linked Data - Sequence & Population

gnomAD v2:

9:22770886 A / G

gnomAD v3:

9:22770887 A / G

gnomAD v4:

chr9-22770887-A-G

Joint Max Group AF 0.42697093 (AMR)

Genomes Max Group AF 0.42697093 (AMR)

Linked Data - NCBI & NCI

dbSNP:

10811771

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22770887A>G , CM000671.2:g.22770887A>G	GRCh38
NC_000009.11:g.22770886A>G , CM000671.1:g.22770886A>G	GRCh37
NC_000009.10:g.22760886A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038977.1:n.524+47457A>G

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