Allele Registry

Canonical Allele Identifier: CA13087162

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.90801254A>G

GRCh37 chr9:g.93563536A>G

Linked Data - Sequence & Population

gnomAD v2:

9:93563536 A / G

gnomAD v3:

9:90801254 A / G

gnomAD v4:

chr9-90801254-A-G

Joint Max Group AF 0.42357151 (EAS)

Genomes Max Group AF 0.42357151 (EAS)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001679460

ClinVar Variation:

1275221

dbSNP:

290986

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.90801254A>G , CM000671.2:g.90801254A>G	GRCh38
NC_000009.11:g.93563536A>G , CM000671.1:g.93563536A>G	GRCh37
NC_000009.10:g.92603357A>G	NCBI36
NG_017046.1:g.4525A>G
NG_017046.2:g.4525A>G

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