Canonical Allele Identifier: CA86186546

Gene: LINC02006

Linked Data

• dbSNP Id: rs564661204
• gnomAD v3: 3-153632348-G-A
• gnomAD v4: 3-153632348-G-A
• MyVariant Identifiers: chr3:g.153350137G>A (hg19) ; chr3:g.153632348G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.153632348G>A , CM000665.2:g.153632348G>A	GRCh38
NC_000003.11:g.153350137G>A , CM000665.1:g.153350137G>A	GRCh37
NC_000003.10:g.154832827G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924593.1:n.363-27603C>T
XR_924594.1:n.60+25722C>T
NR_146713.1:n.161-27603C>T