Canonical Allele Identifier: CA2403319701

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267493G= , CM000684.2:g.35267493G=	GRCh38
NC_000022.10:g.35663486G= , CM000684.1:g.35663486G=	GRCh37
NC_000022.9:g.33993486G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1890G= MANE Select	ENSP00000216106.5:n.1215+1890G=
ENST00000216106.5:c.1215+1890G=	ENSP00000216106.5:n.1215+1890G=
ENST00000418170.5:c.*1051+1890G=	ENSP00000395532.1:n.*1051+1890G=
NM_001003681.2:c.1215+1890G=	NP_001003681.1:n.1215+1890G=
NR_027780.1:n.1504+1890G=
XM_006724100.2:c.1344+1890G=	XP_006724163.1:n.1344+1890G=
XM_006724101.2:c.1344+1890G=	XP_006724164.1:n.1344+1890G=
XM_006724102.1:c.888+1890G=	XP_006724165.1:n.888+1890G=
XM_011529817.1:c.1215+1890G=	XP_011528119.1:n.1215+1890G=
NM_001362972.1:c.888+1890G=	NP_001349901.1:n.888+1890G=
XM_006724100.4:c.1344+1890G=	XP_006724163.1:n.1344+1890G=
XM_006724101.4:c.1344+1890G=	XP_006724164.1:n.1344+1890G=
XM_006724102.2:c.888+1890G=	XP_006724165.1:n.888+1890G=
NM_001003681.3:c.1215+1890G= MANE Select	NP_001003681.1:n.1215+1890G=
NM_001362972.2:c.888+1890G=	NP_001349901.1:n.888+1890G=
NR_027780.2:n.1463+1890G=