Canonical Allele Identifier: CA547266979

Gene: LINC02006

Linked Data

• dbSNP Id: rs1382851075
• gnomAD v2: 3-153350159-T-A
• gnomAD v3: 3-153632370-T-A
• gnomAD v4: 3-153632370-T-A
• MyVariant Identifiers: chr3:g.153350159T>A (hg19) ; chr3:g.153632370T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.153632370T>A , CM000665.2:g.153632370T>A	GRCh38
NC_000003.11:g.153350159T>A , CM000665.1:g.153350159T>A	GRCh37
NC_000003.10:g.154832849T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924593.1:n.363-27625A>T
XR_924594.1:n.60+25700A>T
NR_146713.1:n.161-27625A>T