Allele Registry

Canonical Allele Identifier: CA15723663

Gene:

Linked Data - Expert Curation

COSMIC:

COSN1134838 (not active)

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.56698623C>T

GRCh37 chr11:g.56466099C>T

Linked Data - Sequence & Population

gnomAD v2:

11:56466099 C / T

gnomAD v3:

11:56698623 C / T

gnomAD v4:

chr11-56698623-C-T

Joint Max Group AF 0.70098611 (AFR)

Genomes Max Group AF 0.70098611 (AFR)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001095459

ClinVar Variation:

873251

dbSNP:

1397048

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56698623C>T , CM000673.2:g.56698623C>T	GRCh38
NC_000011.9:g.56466099C>T , CM000673.1:g.56466099C>T	GRCh37
NC_000011.8:g.56222675C>T	NCBI36

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