Allele Registry

Canonical Allele Identifier: CA188478632

Gene:

Linked Data - Expert Curation

COSMIC:

COSN14787490 (not active)

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr9:g.5213687T>C

GRCh37 chr9:g.5213687T>C

Linked Data - Sequence & Population

gnomAD v2:

9:5213687 T / C

gnomAD v3:

9:5213687 T / C

gnomAD v4:

chr9-5213687-T-C

Joint Max Group AF 0.6482333 (AFR)

Genomes Max Group AF 0.6482333 (AFR)

Linked Data - NCBI & NCI

dbSNP:

10975003

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5213687T>C , CM000671.2:g.5213687T>C	GRCh38
NC_000009.11:g.5213687T>C , CM000671.1:g.5213687T>C	GRCh37
NC_000009.10:g.5203687T>C	NCBI36

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