Allele Registry

Canonical Allele Identifier: CA13427637

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.102955810C>T

GRCh37 chr11:g.102826539C>T

Linked Data - Sequence & Population

gnomAD v2:

11:102826539 C / T

gnomAD v3:

11:102955810 C / T

gnomAD v4:

chr11-102955810-C-T

Joint Max Group AF 0.71468475 (AFR)

Genomes Max Group AF 0.71001614 (AFR)

Exomes Max Group AF 0.71590183 (AFR)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001514053

ClinVar Variation:

1166185

dbSNP:

2252070

2119649296

2119649300

2119649325

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102955810C>T , CM000673.2:g.102955810C>T	GRCh38
NC_000011.9:g.102826539C>T , CM000673.1:g.102826539C>T	GRCh37
NC_000011.8:g.102331749C>T	NCBI36
NG_021404.1:g.4925G>A

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