Canonical Allele Identifier: CA323503213

Gene: HMGXB4

Linked Data

• dbSNP Id: rs986891350
• MyVariant Identifiers: chr22:g.35663425A>G (hg19) ; chr22:g.35267432A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267432A>G , CM000684.2:g.35267432A>G	GRCh38
NC_000022.10:g.35663425A>G , CM000684.1:g.35663425A>G	GRCh37
NC_000022.9:g.33993425A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216106.6:c.1215+1829A>G MANE Select	ENSP00000216106.5:n.1215+1829A>G
ENST00000216106.5:c.1215+1829A>G	ENSP00000216106.5:n.1215+1829A>G
ENST00000418170.5:c.*1051+1829A>G	ENSP00000395532.1:n.*1051+1829A>G
NM_001003681.2:c.1215+1829A>G	NP_001003681.1:n.1215+1829A>G
NR_027780.1:n.1504+1829A>G
XM_006724100.2:c.1344+1829A>G	XP_006724163.1:n.1344+1829A>G
XM_006724101.2:c.1344+1829A>G	XP_006724164.1:n.1344+1829A>G
XM_006724102.1:c.888+1829A>G	XP_006724165.1:n.888+1829A>G
XM_011529817.1:c.1215+1829A>G	XP_011528119.1:n.1215+1829A>G
NM_001362972.1:c.888+1829A>G	NP_001349901.1:n.888+1829A>G
XM_006724100.4:c.1344+1829A>G	XP_006724163.1:n.1344+1829A>G
XM_006724101.4:c.1344+1829A>G	XP_006724164.1:n.1344+1829A>G
XM_006724102.2:c.888+1829A>G	XP_006724165.1:n.888+1829A>G
NM_001003681.3:c.1215+1829A>G MANE Select	NP_001003681.1:n.1215+1829A>G
NM_001362972.2:c.888+1829A>G	NP_001349901.1:n.888+1829A>G
NR_027780.2:n.1463+1829A>G