Canonical Allele Identifier: CA1590758479

Gene: HMGXB3

Linked Data

Genomic Alleles

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

Transcript Alleles

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