Allele Registry

Canonical Allele Identifier: CA15216793

Gene: LINC01934 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr2:g.181131318A>G

GRCh37 chr2:g.181996045A>G

Linked Data - Sequence & Population

gnomAD v2:

2:181996045 A / G

gnomAD v3:

2:181131318 A / G

gnomAD v4:

chr2-181131318-A-G

Joint Max Group AF 0.71890455 (EAS)

Genomes Max Group AF 0.71890455 (EAS)

Linked Data - NCBI & NCI

dbSNP:

13010713

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181131318A>G , CM000664.2:g.181131318A>G	GRCh38
NC_000002.11:g.181996045A>G , CM000664.1:g.181996045A>G	GRCh37
NC_000002.10:g.181704290A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130784.1:n.144+7338A>G

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