Allele Registry

Canonical Allele Identifier: CA12160141

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.135990901A>G

GRCh37 chr5:g.135326590A>G

Linked Data - Sequence & Population

gnomAD v2:

5:135326590 A / G

gnomAD v3:

5:135990901 A / G

gnomAD v4:

chr5-135990901-A-G

Joint Max Group AF 0.75287063 (AFR)

Genomes Max Group AF 0.75287063 (AFR)

Linked Data - NCBI & NCI

dbSNP:

30740

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.135990901A>G , CM000667.2:g.135990901A>G	GRCh38
NC_000005.9:g.135326590A>G , CM000667.1:g.135326590A>G	GRCh37
NC_000005.8:g.135354489A>G	NCBI36

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