Allele Registry

Canonical Allele Identifier: CA11985957

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.155476610A>G

GRCh37 chr5:g.154856170A>G

Linked Data - Sequence & Population

gnomAD v2:

5:154856170 A / G

gnomAD v3:

5:155476610 A / G

gnomAD v4:

chr5-155476610-A-G

Joint Max Group AF 0.95150501 (EAS)

Genomes Max Group AF 0.95150501 (EAS)

Linked Data - NCBI & NCI

dbSNP:

267015

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.155476610A>G , CM000667.2:g.155476610A>G	GRCh38
NC_000005.9:g.154856170A>G , CM000667.1:g.154856170A>G	GRCh37
NC_000005.8:g.154836363A>G	NCBI36

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