Allele Registry

Canonical Allele Identifier: CA590217012

Gene:

Linked Data - Expert Curation

COSMIC:

COSN26313360

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.121787363C>G

GRCh37 chr9:g.124549642C>G

Linked Data - Sequence & Population

gnomAD v2:

9:124549642 C / G

gnomAD v3:

9:121787363 C / G

gnomAD v4:

chr9-121787363-C-G

Joint Max Group AF 0.00000802 (AFR)

Genomes Max Group AF 0.00000802 (AFR)

Linked Data - NCBI & NCI

dbSNP:

10985375

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121787363C>G , CM000671.2:g.121787363C>G	GRCh38
NC_000009.11:g.124549642C>G , CM000671.1:g.124549642C>G	GRCh37
NC_000009.10:g.123589463C>G	NCBI36

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