Allele Registry

Canonical Allele Identifier: CA31950561

Gene: LINC01363 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.167187263T>C

GRCh37 chr1:g.167156500T>C

Linked Data - Sequence & Population

gnomAD v2:

1:167156500 T / C

gnomAD v3:

1:167187263 T / C

gnomAD v4:

chr1-167187263-T-C

Joint Max Group AF 0.37406842 (MID)

Genomes Max Group AF 0.37156116 (NFE)

Linked Data - NCBI & NCI

dbSNP:

9803659

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167187263T>C , CM000663.2:g.167187263T>C	GRCh38
NC_000001.10:g.167156500T>C , CM000663.1:g.167156500T>C	GRCh37
NC_000001.9:g.165423124T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110811.1:n.249-5070A>G

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