Allele Registry

Canonical Allele Identifier: CA188993522

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.7558261C>T

GRCh37 chr9:g.7558261C>T

Linked Data - Sequence & Population

gnomAD v2:

9:7558261 C / T

gnomAD v3:

9:7558261 C / T

gnomAD v4:

chr9-7558261-C-T

Joint Max Group AF 0.16899879 (NFE)

Genomes Max Group AF 0.16899879 (NFE)

Linked Data - NCBI & NCI

dbSNP:

4400445

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.7558261C>T , CM000671.2:g.7558261C>T	GRCh38
NC_000009.11:g.7558261C>T , CM000671.1:g.7558261C>T	GRCh37
NC_000009.10:g.7548261C>T	NCBI36

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