Canonical Allele Identifier: CA1381162996
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111815

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495395T>A , CM000665.2:g.86495395T>A GRCh38
NC_000003.11:g.86544545T>A , CM000665.1:g.86544545T>A GRCh37
NC_000003.10:g.86627235T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-396T>A
NR_135563.1:n.116-396T>A