Allele Registry

Canonical Allele Identifier: CA13437480

Gene: LINC02547 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.12050956G>C

GRCh37 chr11:g.12072503G>C

Linked Data - Sequence & Population

gnomAD v2:

11:12072503 G / C

gnomAD v3:

11:12050956 G / C

gnomAD v4:

chr11-12050956-G-C

Joint Max Group AF 0.62635161 (EAS)

Genomes Max Group AF 0.62635161 (EAS)

Linked Data - NCBI & NCI

dbSNP:

923175

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.12050956G>C , CM000673.2:g.12050956G>C	GRCh38
NC_000011.9:g.12072503G>C , CM000673.1:g.12072503G>C	GRCh37
NC_000011.8:g.12029079G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_931035.1:n.57-7578G>C
NR_135109.1:n.57-7578G>C

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