Canonical Allele Identifier: CA227348411

Gene:

Linked Data

• ClinVar Variation Id: 12793
• ClinVar RCV Id: RCV000013637
• dbSNP Id: rs35068180
• gnomAD v2: 11-102715947-G-GA
• gnomAD v3: 11-102845216-G-GA
• gnomAD v4: 11-102845216-G-GA
• MyVariant Identifiers: chr11:g.102715948_102715949insA (hg19) ; chr11:g.102715947_102715948insA (hg19) ; chr11:g.102845217_102845218insA (hg38) ; chr11:g.102845216_102845217insA (hg38)

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