Canonical Allele Identifier: CA686364780

Gene:

Linked Data

• dbSNP Id: rs1298738466
• gnomAD v3: 12-21249994-C-CT
• gnomAD v4: 12-21249994-C-CT
• MyVariant Identifiers: chr12:g.21402928_21402929insT (hg19) ; chr12:g.21249994_21249995insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21249995dup , CM000674.2:g.21249995dup	GRCh38
NC_000012.11:g.21402929dup , CM000674.1:g.21402929dup	GRCh37
NC_000012.10:g.21294196dup	NCBI36