Allele Registry

Canonical Allele Identifier: CA12039397

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.151094113A>G

GRCh37 chr5:g.150473674A>G

Linked Data - Sequence & Population

gnomAD v2:

5:150473674 A / G

gnomAD v3:

5:151094113 A / G

gnomAD v4:

chr5-151094113-A-G

Joint Max Group AF 0.70580432 (EAS)

Genomes Max Group AF 0.70580432 (EAS)

Linked Data - NCBI & NCI

dbSNP:

999556

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151094113A>G , CM000667.2:g.151094113A>G	GRCh38
NC_000005.9:g.150473674A>G , CM000667.1:g.150473674A>G	GRCh37
NC_000005.8:g.150453867A>G	NCBI36

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