Allele Registry

Canonical Allele Identifier: CA11261246

Gene: LINC01934 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.181397142A>G

GRCh37 chr2:g.182261869A>G

Linked Data - Sequence & Population

gnomAD v2:

2:182261869 A / G

gnomAD v3:

2:181397142 A / G

gnomAD v4:

chr2-181397142-A-G

Joint Max Group AF 0.5987675 (NFE)

Genomes Max Group AF 0.5987675 (NFE)

Linked Data - NCBI & NCI

dbSNP:

7602460

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181397142A>G , CM000664.2:g.181397142A>G	GRCh38
NC_000002.11:g.182261869A>G , CM000664.1:g.182261869A>G	GRCh37
NC_000002.10:g.181970114A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130784.1:n.591-1237A>G

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