Canonical Allele Identifier: CA900877359

Gene: LINC02006

Linked Data

• dbSNP Id: rs1250037596
• MyVariant Identifiers: chr3:g.153350053C>T (hg19) ; chr3:g.153632264C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.153632264C>T , CM000665.2:g.153632264C>T	GRCh38
NC_000003.11:g.153350053C>T , CM000665.1:g.153350053C>T	GRCh37
NC_000003.10:g.154832743C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924593.1:n.363-27519G>A
XR_924594.1:n.60+25806G>A
NR_146713.1:n.161-27519G>A