Canonical Allele Identifier: CA86186543

Gene: LINC02006

Linked Data

• dbSNP Id: rs989700811
• gnomAD v2: 3-153350058-T-C
• gnomAD v3: 3-153632269-T-C
• gnomAD v4: 3-153632269-T-C
• MyVariant Identifiers: chr3:g.153350058T>C (hg19) ; chr3:g.153632269T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.153632269T>C , CM000665.2:g.153632269T>C	GRCh38
NC_000003.11:g.153350058T>C , CM000665.1:g.153350058T>C	GRCh37
NC_000003.10:g.154832748T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924593.1:n.363-27524A>G
XR_924594.1:n.60+25801A>G
NR_146713.1:n.161-27524A>G