Canonical Allele Identifier: CA1590758478

Gene: HMGXB3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150027170G= , CM000667.2:g.150027170G=	GRCh38
NC_000005.9:g.149406733G= , CM000667.1:g.149406733G=	GRCh37
NC_000005.8:g.149386926G=	NCBI36
NG_021389.1:g.31565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502717.6:c.1734+53G= MANE Select	ENSP00000421917.1:n.1734+53G=
ENST00000502717.5:c.1734+53G=	ENSP00000421917.1:n.1734+53G=
ENST00000503427.5:c.1638+53G=	ENSP00000422231.1:n.1638+53G=
ENST00000514469.1:c.55+53G=
ENST00000613459.4:c.2472+53G=	ENSP00000479027.1:n.2472+53G=
NM_014983.2:c.1734+53G=	NP_055798.2:n.1734+53G=
XM_006714765.2:c.1236+53G=	XP_006714828.1:n.1236+53G=
XM_006714766.2:c.1137+53G=	XP_006714829.1:n.1137+53G=
NM_001366501.1:c.1236+53G=	NP_001353430.1:n.1236+53G=
XR_001742043.2:n.2305+53G=
NM_014983.3:c.1734+53G= MANE Select	NP_055798.3:n.1734+53G=
NM_001366501.2:c.1236+53G=	NP_001353430.1:n.1236+53G=