Canonical Allele Identifier: CA2403319740

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267615T= , CM000684.2:g.35267615T=	GRCh38
NC_000022.10:g.35663608T= , CM000684.1:g.35663608T=	GRCh37
NC_000022.9:g.33993608T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+2012T= MANE Select	ENSP00000216106.5:n.1215+2012T=
ENST00000216106.5:c.1215+2012T=	ENSP00000216106.5:n.1215+2012T=
ENST00000418170.5:c.*1051+2012T=	ENSP00000395532.1:n.*1051+2012T=
NM_001003681.2:c.1215+2012T=	NP_001003681.1:n.1215+2012T=
NR_027780.1:n.1504+2012T=
XM_006724100.2:c.1344+2012T=	XP_006724163.1:n.1344+2012T=
XM_006724101.2:c.1344+2012T=	XP_006724164.1:n.1344+2012T=
XM_006724102.1:c.888+2012T=	XP_006724165.1:n.888+2012T=
XM_011529817.1:c.1215+2012T=	XP_011528119.1:n.1215+2012T=
NM_001362972.1:c.888+2012T=	NP_001349901.1:n.888+2012T=
XM_006724100.4:c.1344+2012T=	XP_006724163.1:n.1344+2012T=
XM_006724101.4:c.1344+2012T=	XP_006724164.1:n.1344+2012T=
XM_006724102.2:c.888+2012T=	XP_006724165.1:n.888+2012T=
NM_001003681.3:c.1215+2012T= MANE Select	NP_001003681.1:n.1215+2012T=
NM_001362972.2:c.888+2012T=	NP_001349901.1:n.888+2012T=
NR_027780.2:n.1463+2012T=