Allele Registry

Canonical Allele Identifier: CA15152608

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.9557042A>G

GRCh37 chr2:g.9697171A>G

Linked Data - Sequence & Population

gnomAD v2:

2:9697171 A / G

gnomAD v3:

2:9557042 A / G

gnomAD v4:

chr2-9557042-A-G

Joint Max Group AF 0.23953878 (MID)

Genomes Max Group AF 0.20314908 (NFE)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV004780733

ClinVar Variation:

3235267

dbSNP:

11684747

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.9557042A>G , CM000664.2:g.9557042A>G	GRCh38
NC_000002.11:g.9697171A>G , CM000664.1:g.9697171A>G	GRCh37
NC_000002.10:g.9614622A>G	NCBI36
NG_029873.1:g.3747T>C

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