Canonical Allele Identifier: CA86186541

Gene: LINC02006

Linked Data

• dbSNP Id: rs970798025
• gnomAD v2: 3-153350036-C-T
• gnomAD v3: 3-153632247-C-T
• gnomAD v4: 3-153632247-C-T
• MyVariant Identifiers: chr3:g.153350036C>T (hg19) ; chr3:g.153632247C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.153632247C>T , CM000665.2:g.153632247C>T	GRCh38
NC_000003.11:g.153350036C>T , CM000665.1:g.153350036C>T	GRCh37
NC_000003.10:g.154832726C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924593.1:n.363-27502G>A
XR_924594.1:n.60+25823G>A
NR_146713.1:n.161-27502G>A