Allele Registry

Canonical Allele Identifier: CA15401999

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.108580035A>G

GRCh37 chr5:g.107915736A>G

Linked Data - Sequence & Population

gnomAD v2:

5:107915736 A / G

gnomAD v3:

5:108580035 A / G

gnomAD v4:

chr5-108580035-A-G

Joint Max Group AF 0.85295393 (AFR)

Genomes Max Group AF 0.85295393 (AFR)

Linked Data - NCBI & NCI

dbSNP:

10447248

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108580035A>G , CM000667.2:g.108580035A>G	GRCh38
NC_000005.9:g.107915736A>G , CM000667.1:g.107915736A>G	GRCh37
NC_000005.8:g.107943635A>G	NCBI36

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