Allele Registry

Canonical Allele Identifier: CA227348411

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.102845217_102845218insA

GRCh38 chr11:g.102845216_102845217insA

GRCh37 chr11:g.102715948_102715949insA

GRCh37 chr11:g.102715947_102715948insA

Linked Data - Sequence & Population

gnomAD v2:

11:102715947 G / GA

gnomAD v3:

11:102845216 G / GA

gnomAD v4:

chr11-102845216-G-GA

Joint Max Group AF 0.88490929 (AFR)

Genomes Max Group AF 0.88490929 (AFR)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013637

ClinVar Variation:

12793

dbSNP:

35068180

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102845221dup , CM000673.2:g.102845221dup	GRCh38
NC_000011.9:g.102715952dup , CM000673.1:g.102715952dup	GRCh37
NC_000011.8:g.102221162dup	NCBI36
NG_012100.1:g.3395dup

Search 100 bp 5'

Search 100 bp 3'