Allele Registry

Canonical Allele Identifier: CA113506399

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.4199820C>G

GRCh37 chr5:g.4199933C>G

Linked Data - Sequence & Population

gnomAD v2:

5:4199933 C / G

gnomAD v3:

5:4199820 C / G

gnomAD v4:

chr5-4199820-C-G

Joint Max Group AF 0.97143807 (EAS)

Genomes Max Group AF 0.97143807 (EAS)

Linked Data - NCBI & NCI

dbSNP:

10036225

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.4199820C>G , CM000667.2:g.4199820C>G	GRCh38
NC_000005.9:g.4199933C>G , CM000667.1:g.4199933C>G	GRCh37
NC_000005.8:g.4252933C>G	NCBI36

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