Allele Registry

Canonical Allele Identifier: CA11025141

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr2:g.112837290A>G

GRCh37 chr2:g.113594867A>G

Linked Data - Sequence & Population

gnomAD v2:

2:113594867 A / G

gnomAD v3:

2:112837290 A / G

gnomAD v4:

chr2-112837290-A-G

Joint Max Group AF 0.66089847 (NFE)

Genomes Max Group AF 0.66089847 (NFE)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001078162

ClinVar Variation:

869138

dbSNP:

16944

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112837290A>G , CM000664.2:g.112837290A>G	GRCh38
NC_000002.11:g.113594867A>G , CM000664.1:g.113594867A>G	GRCh37
NC_000002.10:g.113311338A>G	NCBI36
NG_008851.1:g.4490T>C

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