Allele Registry

Canonical Allele Identifier: CA212296886

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.102837961G>T

GRCh37 chr10:g.104597718G>T

Linked Data - Sequence & Population

gnomAD v2:

10:104597718 G / T

gnomAD v3:

10:102837961 G / T

gnomAD v4:

chr10-102837961-G-T

Joint Max Group AF 0.06314846 (EAS)

Genomes Max Group AF 0.06432303 (EAS)

Exomes Max Group AF 0.042626 (EAS)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001513266

ClinVar Variation:

1165814

dbSNP:

17115149

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837961G>T , CM000672.2:g.102837961G>T	GRCh38
NC_000010.10:g.104597718G>T , CM000672.1:g.104597718G>T	GRCh37
NC_000010.9:g.104587708G>T	NCBI36
NG_007955.1:g.4573C>A

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