Allele Registry

Canonical Allele Identifier: CA10750792

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr1:g.211317810A>G

GRCh37 chr1:g.211491152A>G

Linked Data - Sequence & Population

gnomAD v2:

1:211491152 A / G

gnomAD v3:

1:211317810 A / G

gnomAD v4:

chr1-211317810-A-G

Joint Max Group AF 0.902426 (NFE)

Genomes Max Group AF 0.902426 (NFE)

Linked Data - NCBI & NCI

dbSNP:

6540679

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211317810A>G , CM000663.2:g.211317810A>G	GRCh38
NC_000001.10:g.211491152A>G , CM000663.1:g.211491152A>G	GRCh37
NC_000001.9:g.209557775A>G	NCBI36

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