Canonical Allele Identifier: CA691086168

Gene:

Linked Data

• dbSNP Id: rs72011118
• gnomAD v3: 12-66000732-T-TTG
• gnomAD v4: 12-66000732-T-TTG
• MyVariant Identifiers: chr12:g.66394512_66394513insTG (hg19) ; chr12:g.66000732_66000733insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66000786_66000787dup , CM000674.2:g.66000786_66000787dup	GRCh38
NC_000012.11:g.66394566_66394567dup , CM000674.1:g.66394566_66394567dup	GRCh37
NC_000012.10:g.64680833_64680834dup	NCBI36