Canonical Allele Identifier: CA13528665

Gene: LINC02751

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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