Canonical Allele Identifier: CA2177601263
Gene: LINC02490 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.52987181A= , CM000677.2:g.52987181A= GRCh38
NC_000015.9:g.53279378A= , CM000677.1:g.53279378A= GRCh37
NC_000015.8:g.51066670A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932256.1:n.463+11332A=
XR_932257.1:n.463+11332A=
XM_017022782.1:c.*4896A= XP_016878271.1:n.*4896A=
XM_017022783.1:c.*4896A= XP_016878272.1:n.*4896A=
XM_017022784.1:c.451+11332A= XP_016878273.1:n.451+11332A=
XM_017022785.1:c.451+11332A= XP_016878274.1:n.451+11332A=
XR_001751547.1:n.5434A=
XR_001751548.1:n.552+11332A=
XR_932257.2:n.533+11332A=
XR_004837528.1:n.5584A=
XR_004837529.1:n.5519A=
XR_004837530.1:n.533+11332A=
XR_004837531.1:n.533+11332A=