Canonical Allele Identifier: CA752363629

Gene: OSBP2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30757289G>T , CM000684.2:g.30757289G>T	GRCh38
NC_000022.10:g.31153276G>T , CM000684.1:g.31153276G>T	GRCh37
NC_000022.9:g.29483276G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332585.11:c.853+15920G>T MANE Select	ENSP00000332576.6:n.853+15920G>T
ENST00000332585.10:c.853+15920G>T	ENSP00000332576.6:n.853+15920G>T
ENST00000403222.7:c.16+15920G>T	ENSP00000384213.4:n.16+15920G>T
ENST00000407373.5:c.334+15920G>T	ENSP00000385237.1:n.334+15920G>T
ENST00000438716.3:c.358+15920G>T	ENSP00000411052.2:n.358+15920G>T
ENST00000446658.6:c.853+15920G>T	ENSP00000392080.2:n.853+15920G>T
NM_001282738.1:c.358+15920G>T	NP_001269667.1:n.358+15920G>T
NM_001282739.1:c.853+15920G>T	NP_001269668.1:n.853+15920G>T
NM_030758.3:c.853+15920G>T	NP_110385.1:n.853+15920G>T
XM_005261465.3:c.853+15920G>T	XP_005261522.1:n.853+15920G>T
XM_006724203.2:c.853+15920G>T	XP_006724266.2:n.853+15920G>T
XM_011530057.1:c.853+15920G>T	XP_011528359.1:n.853+15920G>T
XM_011530058.1:c.853+15920G>T	XP_011528360.1:n.853+15920G>T
XM_011530059.1:c.853+15920G>T	XP_011528361.1:n.853+15920G>T
NM_030758.4:c.853+15920G>T MANE Select	NP_110385.1:n.853+15920G>T
NM_001282739.2:c.853+15920G>T	NP_001269668.1:n.853+15920G>T
NM_001282738.2:c.358+15920G>T	NP_001269667.1:n.358+15920G>T