Allele Registry

Canonical Allele Identifier: CA113616893

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.5091915A>G

GRCh37 chr5:g.5092028A>G

Linked Data - Sequence & Population

gnomAD v2:

5:5092028 A / G

gnomAD v3:

5:5091915 A / G

gnomAD v4:

chr5-5091915-A-G

Joint Max Group AF 0.45001672 (MID)

Genomes Max Group AF 0.3907705 (NFE)

Linked Data - NCBI & NCI

dbSNP:

1824938

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.5091915A>G , CM000667.2:g.5091915A>G	GRCh38
NC_000005.9:g.5092028A>G , CM000667.1:g.5092028A>G	GRCh37
NC_000005.8:g.5145028A>G	NCBI36

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