Canonical Allele Identifier: CA13333591

Gene: LDB3

Linked Data

• ClinVar Variation Id: 669632
• ClinVar RCV Id: RCV000828715
• dbSNP Id: rs34073498
• gnomAD v2: 10-88428036-A-G
• gnomAD v3: 10-86668279-A-G
• gnomAD v4: 10-86668279-A-G
• MyVariant Identifiers: chr10:g.88428036A>G (hg19) ; chr10:g.86668279A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86668279A>G , CM000672.2:g.86668279A>G	GRCh38
NC_000010.10:g.88428036A>G , CM000672.1:g.88428036A>G	GRCh37
NC_000010.9:g.88418016A>G	NCBI36
NG_008876.1:g.4716A>G , LRG_385:g.4716A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443292.2:c.1487-390A>G	ENSP00000393132.2:n.1487-390A>G
ENST00000685347.1:n.1449-390A>G
ENST00000687856.1:c.-23-390A>G	ENSP00000510221.1:n.-23-390A>G
ENST00000688001.1:c.-23-390A>G	ENSP00000508987.1:n.-23-390A>G
ENST00000688785.1:c.-23-390A>G	ENSP00000509572.1:n.-23-390A>G
ENST00000691462.1:c.-23-390A>G	ENSP00000509930.1:n.-23-390A>G
ENST00000692941.1:n.2070-390A>G
XM_011539185.1:c.-23-390A>G	XP_011537487.1:n.-23-390A>G
XM_011539189.1:c.-23-390A>G	XP_011537491.1:n.-23-390A>G
XM_011539193.1:c.-495-390A>G	XP_011537495.1:n.-495-390A>G
XM_011539194.1:c.-495-390A>G	XP_011537496.1:n.-495-390A>G
XM_011539185.2:c.-23-390A>G	XP_011537487.1:n.-23-390A>G
XM_017015606.1:c.-23-390A>G	XP_016871095.1:n.-23-390A>G
XM_017015608.1:c.-23-390A>G	XP_016871097.1:n.-23-390A>G
XM_017015609.1:c.-23-390A>G	XP_016871098.1:n.-23-390A>G
NM_001368063.1:c.-23-390A>G	NP_001354992.1:n.-23-390A>G
NM_001368064.1:c.-23-390A>G	NP_001354993.1:n.-23-390A>G
NM_001368068.1:c.-23-390A>G	NP_001354997.1:n.-23-390A>G