Allele Registry

Canonical Allele Identifier: CA227767534

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.104463511A>G

GRCh37 chr11:g.104334239A>G

Linked Data - Sequence & Population

gnomAD v2:

11:104334239 A / G

gnomAD v3:

11:104463511 A / G

gnomAD v4:

chr11-104463511-A-G

Joint Max Group AF 0.18938271 (AFR)

Genomes Max Group AF 0.18938271 (AFR)

Linked Data - NCBI & NCI

dbSNP:

11226373

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.104463511A>G , CM000673.2:g.104463511A>G	GRCh38
NC_000011.9:g.104334239A>G , CM000673.1:g.104334239A>G	GRCh37
NC_000011.8:g.103839449A>G	NCBI36

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