Allele Registry

Canonical Allele Identifier: CA11145219

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.9581767C>A

GRCh37 chr2:g.9721896C>A

Linked Data - Sequence & Population

gnomAD v2:

2:9721896 C / A

gnomAD v3:

2:9581767 C / A

gnomAD v4:

chr2-9581767-C-A

Joint Max Group AF 0.8081943 (AFR)

Genomes Max Group AF 0.8081943 (AFR)

Linked Data - NCBI & NCI

dbSNP:

6432018

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.9581767C>A , CM000664.2:g.9581767C>A	GRCh38
NC_000002.11:g.9721896C>A , CM000664.1:g.9721896C>A	GRCh37
NC_000002.10:g.9639347C>A	NCBI36

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