Canonical Allele Identifier: CA900877337

Gene: LINC02006

Linked Data

• dbSNP Id: rs1417810214
• gnomAD v3: 3-153632228-A-AT
• gnomAD v4: 3-153632228-A-AT
• MyVariant Identifiers: chr3:g.153350017_153350018insT (hg19) ; chr3:g.153632228_153632229insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.153632228_153632229insT , CM000665.2:g.153632228_153632229insT	GRCh38
NC_000003.11:g.153350017_153350018insT , CM000665.1:g.153350017_153350018insT	GRCh37
NC_000003.10:g.154832707_154832708insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924593.1:n.363-27484_363-27483insA
XR_924594.1:n.60+25841_60+25842insA
NR_146713.1:n.161-27484_161-27483insA