Allele Registry

Canonical Allele Identifier: CA13152542

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.42952399A>G

GRCh38 chr10:g.42952399_42952400delinsGT

GRCh37 chr10:g.43447847A>G

GRCh37 chr10:g.43447847_43447848delinsGT

Linked Data - Sequence & Population

gnomAD v2:

10:43447847 A / G

gnomAD v3:

10:42952399 A / G

gnomAD v4:

chr10-42952399-A-G

Joint Max Group AF 0.69639148 (EAS)

Genomes Max Group AF 0.69639148 (EAS)

Linked Data - NCBI & NCI

dbSNP:

2506030

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.42952399A>G , CM000672.2:g.42952399A>G	GRCh38
NC_000010.10:g.43447847A>G , CM000672.1:g.43447847A>G	GRCh37
NC_000010.9:g.42767853A>G	NCBI36

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