Canonical Allele Identifier: CA1204113358

Gene: PBX1

Linked Data

• dbSNP Id: rs1664344733

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.164720498C>T , CM000663.2:g.164720498C>T	GRCh38
NC_000001.10:g.164689735C>T , CM000663.1:g.164689735C>T	GRCh37
NC_000001.9:g.162956359C>T	NCBI36
NG_028246.1:g.166139C>T
NG_028246.2:g.166139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699845.1:c.266-71996C>T	ENSP00000514643.1:n.266-71996C>T
ENST00000699846.1:c.-51+20450C>T	ENSP00000514644.1:n.-51+20450C>T
ENST00000699847.1:c.-51+19787C>T	ENSP00000514645.1:n.-51+19787C>T
ENST00000420696.7:c.266-71996C>T MANE Select	ENSP00000405890.2:n.266-71996C>T
ENST00000340699.7:c.266-71996C>T	ENSP00000341455.3:n.266-71996C>T
ENST00000367897.5:c.266-71996C>T	ENSP00000356872.1:n.266-71996C>T
ENST00000420696.6:c.266-71996C>T	ENSP00000405890.1:n.266-71996C>T
ENST00000468104.5:n.396-71996C>T
ENST00000482110.5:c.-50-71996C>T	ENSP00000453163.1:n.-50-71996C>T
ENST00000496120.6:n.86-71996C>T
ENST00000558796.2:n.244+68359C>T
ENST00000559240.5:c.266-71996C>T	ENSP00000453188.1:n.266-71996C>T
ENST00000559578.1:c.50-71996C>T	ENSP00000452804.1:n.50-71996C>T
ENST00000560469.5:n.222-71996C>T
ENST00000560641.5:c.-51+63126C>T	ENSP00000452727.1:n.-51+63126C>T
ENST00000627490.2:c.266-71996C>T	ENSP00000485692.1:n.266-71996C>T
NM_001204961.1:c.266-71996C>T	NP_001191890.1:n.266-71996C>T
NM_001204963.1:c.266-71996C>T	NP_001191892.1:n.266-71996C>T
NM_002585.3:c.266-71996C>T	NP_002576.1:n.266-71996C>T
XM_005245228.2:c.434-71996C>T	XP_005245285.1:n.434-71996C>T
XM_005245229.2:c.266-71996C>T	XP_005245286.1:n.266-71996C>T
XM_005245230.2:c.-51+19787C>T	XP_005245287.1:n.-51+19787C>T
XM_011509590.1:c.434-71996C>T	XP_011507892.1:n.434-71996C>T
XM_011509591.1:c.434-71996C>T	XP_011507893.1:n.434-71996C>T
XM_011509592.1:c.434-71996C>T	XP_011507894.1:n.434-71996C>T
XM_011509593.1:c.86-71996C>T	XP_011507895.1:n.86-71996C>T
XM_011509594.1:c.-50-71996C>T	XP_011507896.1:n.-50-71996C>T
NM_001353130.1:c.17-71996C>T	NP_001340059.1:n.17-71996C>T
NM_001353131.1:c.266-71996C>T	NP_001340060.1:n.266-71996C>T
XM_005245228.3:c.434-71996C>T	XP_005245285.1:n.434-71996C>T
XM_005245229.3:c.266-71996C>T	XP_005245286.1:n.266-71996C>T
XM_011509590.2:c.434-71996C>T	XP_011507892.1:n.434-71996C>T
XM_011509591.2:c.434-71996C>T	XP_011507893.1:n.434-71996C>T
XM_011509592.2:c.434-71996C>T	XP_011507894.1:n.434-71996C>T
XM_017001395.2:c.266-71996C>T	XP_016856884.1:n.266-71996C>T
NM_002585.4:c.266-71996C>T MANE Select	NP_002576.1:n.266-71996C>T
NM_001204961.2:c.266-71996C>T	NP_001191890.1:n.266-71996C>T
NM_001204963.2:c.266-71996C>T	NP_001191892.1:n.266-71996C>T
NM_001353131.2:c.266-71996C>T	NP_001340060.1:n.266-71996C>T