Canonical Allele Identifier: CA244856522

Gene:

Linked Data

• dbSNP Id: rs34541078
• gnomAD v2: 12-116211914-CTTT-C
• gnomAD v3: 12-115774109-CTTT-C
• gnomAD v4: 12-115774109-CTTT-C
• MyVariant Identifiers: chr12:g.116211917_116211919del (hg19) ; chr12:g.116211915_116211917del (hg19) ; chr12:g.115774112_115774114del (hg38) ; chr12:g.115774110_115774112del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115774130_115774132del , CM000674.2:g.115774130_115774132del	GRCh38
NC_000012.11:g.116211935_116211937del , CM000674.1:g.116211935_116211937del	GRCh37
NC_000012.10:g.114696318_114696320del	NCBI36