Allele Registry

Canonical Allele Identifier: CA14766344

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr20:g.157259T>G

GRCh37 chr20:g.137900T>G

Linked Data - Sequence & Population

gnomAD v2:

20:137900 T / G

gnomAD v3:

20:157259 T / G

gnomAD v4:

chr20-157259-T-G

Joint Max Group AF 0.50067634 (EAS)

Genomes Max Group AF 0.50067634 (EAS)

Linked Data - NCBI & NCI

dbSNP:

1434789

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.157259T>G , CM000682.2:g.157259T>G	GRCh38
NC_000020.10:g.137900T>G , CM000682.1:g.137900T>G	GRCh37
NC_000020.9:g.85900T>G	NCBI36

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