Allele Registry

Canonical Allele Identifier: CA337476390

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrY:g.4210176C>G

GRCh37 chrY:g.4078217C>G

Linked Data - Sequence & Population

gnomAD v3:

Y:4210176 C / G

gnomAD v4:

chrY-4210176-C-G

Joint Max Group AF 0.01608757 (EAS)

Genomes Max Group AF 0.01608757 (EAS)

Linked Data - NCBI & NCI

dbSNP:

3898

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.4210176C>G , CM000686.2:g.4210176C>G	GRCh38
NC_000024.9:g.4078217C>G , CM000686.1:g.4078217C>G	GRCh37
NC_000024.8:g.4138217C>G	NCBI36

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