Allele Registry

Canonical Allele Identifier: CA14935032

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr22:g.21628051C>G

GRCh37 chr22:g.21982340C>G

Linked Data - Sequence & Population

gnomAD v2:

22:21982340 C / G

gnomAD v3:

22:21628051 C / G

gnomAD v4:

chr22-21628051-C-G

Joint Max Group AF 0.64579709 (AFR)

Genomes Max Group AF 0.64547112 (AFR)

Exomes Max Group AF 0.62270465 (AFR)

Linked Data - NCBI & NCI

dbSNP:

861857

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21628051C>G , CM000684.2:g.21628051C>G	GRCh38
NC_000022.10:g.21982340C>G , CM000684.1:g.21982340C>G	GRCh37
NC_000022.9:g.20312340C>G	NCBI36

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