Canonical Allele Identifier: CA606951332

Gene:

Linked Data

• dbSNP Id: rs1399346073
• gnomAD v2: 12-93687173-A-AT
• gnomAD v3: 12-93293397-A-AT
• gnomAD v4: 12-93293397-A-AT
• MyVariant Identifiers: chr12:g.93687173_93687174insT (hg19) ; chr12:g.93293397_93293398insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93293398dup , CM000674.2:g.93293398dup	GRCh38
NC_000012.11:g.93687174dup , CM000674.1:g.93687174dup	GRCh37
NC_000012.10:g.92211305dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040096.1:n.329+34629dup