Allele Registry

Canonical Allele Identifier: CA12713785

Gene: LINC00529 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr8:g.11261528C>T

GRCh38 chr8:g.11261528_11261529delinsTA

GRCh37 chr8:g.11119037C>T

GRCh37 chr8:g.11119037_11119038delinsTA

Linked Data - Sequence & Population

gnomAD v2:

8:11119037 C / T

gnomAD v3:

8:11261528 C / T

gnomAD v4:

chr8-11261528-C-T

Joint Max Group AF 0.16411908 (NFE)

Genomes Max Group AF 0.16411908 (NFE)

Linked Data - NCBI & NCI

dbSNP:

2251301

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11261528C>T , CM000670.2:g.11261528C>T	GRCh38
NC_000008.10:g.11119037C>T , CM000670.1:g.11119037C>T	GRCh37
NC_000008.9:g.11156447C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170283.1:n.558+6261G>A

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