Canonical Allele Identifier: CA514323741

Gene: HMGXB4

Linked Data

• dbSNP Id: rs1601628381
• MyVariant Identifiers: chr22:g.35663142T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267149T>A , CM000684.2:g.35267149T>A	GRCh38
NC_000022.10:g.35663142T>A , CM000684.1:g.35663142T>A	GRCh37
NC_000022.9:g.33993142T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1546T>A MANE Select	ENSP00000216106.5:n.1215+1546T>A
ENST00000216106.5:c.1215+1546T>A	ENSP00000216106.5:n.1215+1546T>A
ENST00000418170.5:c.*1051+1546T>A	ENSP00000395532.1:n.*1051+1546T>A
NM_001003681.2:c.1215+1546T>A	NP_001003681.1:n.1215+1546T>A
NR_027780.1:n.1504+1546T>A
XM_006724100.2:c.1344+1546T>A	XP_006724163.1:n.1344+1546T>A
XM_006724101.2:c.1344+1546T>A	XP_006724164.1:n.1344+1546T>A
XM_006724102.1:c.888+1546T>A	XP_006724165.1:n.888+1546T>A
XM_011529817.1:c.1215+1546T>A	XP_011528119.1:n.1215+1546T>A
NM_001362972.1:c.888+1546T>A	NP_001349901.1:n.888+1546T>A
XM_006724100.4:c.1344+1546T>A	XP_006724163.1:n.1344+1546T>A
XM_006724101.4:c.1344+1546T>A	XP_006724164.1:n.1344+1546T>A
XM_006724102.2:c.888+1546T>A	XP_006724165.1:n.888+1546T>A
NM_001003681.3:c.1215+1546T>A MANE Select	NP_001003681.1:n.1215+1546T>A
NM_001362972.2:c.888+1546T>A	NP_001349901.1:n.888+1546T>A
NR_027780.2:n.1463+1546T>A