Allele Registry

Canonical Allele Identifier: CA290467875

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr17:g.36463349T>C

Linked Data - Sequence & Population

gnomAD v3:

17:36463349 T / C

gnomAD v4:

chr17-36463349-T-C

Joint Max Group AF 0.79820754 (AFR)

Genomes Max Group AF 0.79820754 (AFR)

Linked Data - NCBI & NCI

dbSNP:

4796217

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.36463349T>C , CM000679.2:g.36463349T>C	GRCh38

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