Canonical Allele Identifier: CA1954337262
Gene: LINC02751 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.15672916G= , CM000673.2:g.15672916G= GRCh38
NC_000011.9:g.15694462G= , CM000673.1:g.15694462G= GRCh37
NC_000011.8:g.15651038G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001293172.1:c.106+28881G= NP_001280101.1:n.106+28881G=
XM_011519838.1:c.106+28881G= XP_011518140.1:n.106+28881G=
XM_011519839.1:c.106+28881G= XP_011518141.1:n.106+28881G=
XM_011519838.3:c.106+28881G= XP_011518140.1:n.106+28881G=
XM_011519839.2:c.106+28881G= XP_011518141.1:n.106+28881G=
NR_169502.1:n.756+28881G=
NR_169503.1:n.770+28881G=
NR_169507.1:n.84-31417G=
NR_169508.1:n.493+28881G=
NR_169509.1:n.252+28881G=