Allele Registry

Canonical Allele Identifier: CA30439166

Gene: LINC02798 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.121458637G>T

Linked Data - Sequence & Population

gnomAD v3:

1:121458637 G / T

gnomAD v4:

chr1-121458637-G-T

Joint Max Group AF 0.78835579 (EAS)

Genomes Max Group AF 0.78835579 (EAS)

Linked Data - NCBI & NCI

dbSNP:

6600671

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.121458637G>T , CM000663.2:g.121458637G>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
XR_001738201.1:n.210-1382G>T

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