Allele Registry

Canonical Allele Identifier: CA181254379

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr8:g.89811459A>G

GRCh37 chr8:g.90823687A>G

Linked Data - Sequence & Population

gnomAD v2:

8:90823687 A / G

gnomAD v3:

8:89811459 A / G

gnomAD v4:

chr8-89811459-A-G

Joint Max Group AF 0.73351675 (AFR)

Genomes Max Group AF 0.73351675 (AFR)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV002291823

ClinVar Variation:

1710536

dbSNP:

40457

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89811459A>G , CM000670.2:g.89811459A>G	GRCh38
NC_000008.10:g.90823687A>G , CM000670.1:g.90823687A>G	GRCh37
NC_000008.9:g.90892832A>G	NCBI36

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