Allele Registry

Canonical Allele Identifier: CA10587001

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr7:g.92528572A>G

GRCh37 chr7:g.92157886A>G

Linked Data - Sequence & Population

gnomAD v2:

7:92157886 A / G

gnomAD v3:

7:92528572 A / G

gnomAD v4:

chr7-92528572-A-G

Joint Max Group AF 0.13278215 (AFR)

Genomes Max Group AF 0.13155028 (AFR)

Exomes Max Group AF 0.1323313 (AFR)

Linked Data - NCBI & NCI

ClinVar Allele:

252977

ClinVar RCV:

RCV000250369

RCV001277066

RCV001532819

RCV001682980

ClinVar Variation:

256215

dbSNP:

12386601

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92528572A>G , CM000669.2:g.92528572A>G	GRCh38
NC_000007.13:g.92157886A>G , CM000669.1:g.92157886A>G	GRCh37
NC_000007.12:g.91995822A>G	NCBI36
NG_008341.1:g.4960T>C
NG_008341.2:g.4960T>C

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