Canonical Allele Identifier: CA57819297

Gene:

Linked Data

• dbSNP Id: rs56796173
• gnomAD v2: 2-145359768-A-ACGTG
• gnomAD v3: 2-144602201-A-ACGTG
• gnomAD v4: 2-144602201-A-ACGTG
• MyVariant Identifiers: chr2:g.145359769_145359770insGTGC (hg19) ; chr2:g.145359768_145359769insCGTG (hg19) ; chr2:g.144602202_144602203insGTGC (hg38) ; chr2:g.144602201_144602202insCGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144602202_144602203insGTGC , CM000664.2:g.144602202_144602203insGTGC	GRCh38
NC_000002.11:g.145359769_145359770insGTGC , CM000664.1:g.145359769_145359770insGTGC	GRCh37
NC_000002.10:g.145076239_145076240insGTGC	NCBI36