Canonical Allele Identifier: CA544492155

Gene: LINC02070

Linked Data

• dbSNP Id: rs1404306574
• gnomAD v2: 3-86544456-TGG-T
• gnomAD v3: 3-86495306-TGG-T
• gnomAD v4: 3-86495306-TGG-T
• MyVariant Identifiers: chr3:g.86544457_86544458del (hg19) ; chr3:g.86544457_86544459delinsA (hg19) ; chr3:g.86495307_86495308del (hg38) ; chr3:g.86495307_86495309delinsA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495307_86495308del , CM000665.2:g.86495307_86495308del	GRCh38
NC_000003.11:g.86544457_86544458del , CM000665.1:g.86544457_86544458del	GRCh37
NC_000003.10:g.86627147_86627148del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-484_116-483del
NR_135563.1:n.116-484_116-483del