Allele Registry

Canonical Allele Identifier: CA13230186

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.117801913T>C

GRCh37 chr10:g.119561424T>C

Linked Data - Sequence & Population

gnomAD v2:

10:119561424 T / C

gnomAD v3:

10:117801913 T / C

gnomAD v4:

chr10-117801913-T-C

Joint Max Group AF 0.56650726 (NFE)

Genomes Max Group AF 0.56650726 (NFE)

Linked Data - NCBI & NCI

dbSNP:

10886142

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117801913T>C , CM000672.2:g.117801913T>C	GRCh38
NC_000010.10:g.119561424T>C , CM000672.1:g.119561424T>C	GRCh37
NC_000010.9:g.119551414T>C	NCBI36

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