Allele Registry

Canonical Allele Identifier: CA197961810

Gene: LINC01492 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.103261938T>C

GRCh37 chr9:g.106024220T>C

Linked Data - Sequence & Population

gnomAD v2:

9:106024220 T / C

gnomAD v3:

9:103261938 T / C

gnomAD v4:

chr9-103261938-T-C

Joint Max Group AF 0.31928226 (EAS)

Genomes Max Group AF 0.31928226 (EAS)

Linked Data - NCBI & NCI

dbSNP:

16922670

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261938T>C , CM000671.2:g.103261938T>C	GRCh38
NC_000009.11:g.106024220T>C , CM000671.1:g.106024220T>C	GRCh37
NC_000009.10:g.105064041T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2586A>G

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