Allele Registry

Canonical Allele Identifier: CA191256932

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.22134151A>T

GRCh37 chr9:g.22134150A>T

Linked Data - Sequence & Population

gnomAD v2:

9:22134150 A / T

gnomAD v3:

9:22134151 A / T

gnomAD v4:

chr9-22134151-A-T

Joint Max Group AF 0.00056222 (AFR)

Genomes Max Group AF 0.00056222 (AFR)

Linked Data - NCBI & NCI

dbSNP:

972354729

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22134151A>T , CM000671.2:g.22134151A>T	GRCh38
NC_000009.11:g.22134150A>T , CM000671.1:g.22134150A>T	GRCh37
NC_000009.10:g.22124150A>T	NCBI36

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