Canonical Allele Identifier: CA559271203

Gene:

Linked Data

• dbSNP Id: rs1197930005
• gnomAD v2: 5-40414970-T-TGTG
• gnomAD v3: 5-40414868-T-TGTG
• gnomAD v4: 5-40414868-T-TGTG
• MyVariant Identifiers: chr5:g.40414976_40414977insGTG (hg19) ; chr5:g.40414970_40414971insGTG (hg19) ; chr5:g.40414874_40414875insGTG (hg38) ; chr5:g.40414868_40414869insGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40414898_40414900dup , CM000667.2:g.40414898_40414900dup	GRCh38
NC_000005.9:g.40415000_40415002dup , CM000667.1:g.40415000_40415002dup	GRCh37
NC_000005.8:g.40450757_40450759dup	NCBI36