Allele Registry

Canonical Allele Identifier: CA192563032

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.31419917G>C

GRCh37 chr9:g.31419915G>C

Linked Data - Sequence & Population

gnomAD v2:

9:31419915 G / C

gnomAD v3:

9:31419917 G / C

gnomAD v4:

chr9-31419917-G-C

Joint Max Group AF 0.265181 (EAS)

Genomes Max Group AF 0.265181 (EAS)

Linked Data - NCBI & NCI

dbSNP:

10435736

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.31419917G>C , CM000671.2:g.31419917G>C	GRCh38
NC_000009.11:g.31419915G>C , CM000671.1:g.31419915G>C	GRCh37
NC_000009.10:g.31409915G>C	NCBI36

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