Canonical Allele Identifier: CA2403319735
Gene: HMGXB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35267605T= , CM000684.2:g.35267605T= GRCh38
NC_000022.10:g.35663598T= , CM000684.1:g.35663598T= GRCh37
NC_000022.9:g.33993598T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216106.6:c.1215+2002T= MANE Select ENSP00000216106.5:n.1215+2002T=
ENST00000216106.5:c.1215+2002T= ENSP00000216106.5:n.1215+2002T=
ENST00000418170.5:c.*1051+2002T= ENSP00000395532.1:n.*1051+2002T=
NM_001003681.2:c.1215+2002T= NP_001003681.1:n.1215+2002T=
NR_027780.1:n.1504+2002T=
XM_006724100.2:c.1344+2002T= XP_006724163.1:n.1344+2002T=
XM_006724101.2:c.1344+2002T= XP_006724164.1:n.1344+2002T=
XM_006724102.1:c.888+2002T= XP_006724165.1:n.888+2002T=
XM_011529817.1:c.1215+2002T= XP_011528119.1:n.1215+2002T=
NM_001362972.1:c.888+2002T= NP_001349901.1:n.888+2002T=
XM_006724100.4:c.1344+2002T= XP_006724163.1:n.1344+2002T=
XM_006724101.4:c.1344+2002T= XP_006724164.1:n.1344+2002T=
XM_006724102.2:c.888+2002T= XP_006724165.1:n.888+2002T=
NM_001003681.3:c.1215+2002T= MANE Select NP_001003681.1:n.1215+2002T=
NM_001362972.2:c.888+2002T= NP_001349901.1:n.888+2002T=
NR_027780.2:n.1463+2002T=