Canonical Allele Identifier: CA547266978

Gene: LINC02006

Linked Data

• dbSNP Id: rs1289091842
• gnomAD v2: 3-153350067-A-G
• gnomAD v3: 3-153632278-A-G
• gnomAD v4: 3-153632278-A-G
• MyVariant Identifiers: chr3:g.153350067A>G (hg19) ; chr3:g.153632278A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.153632278A>G , CM000665.2:g.153632278A>G	GRCh38
NC_000003.11:g.153350067A>G , CM000665.1:g.153350067A>G	GRCh37
NC_000003.10:g.154832757A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924593.1:n.363-27533T>C
XR_924594.1:n.60+25792T>C
NR_146713.1:n.161-27533T>C