Canonical Allele Identifier: CA1925609331

Gene: LDB3

Linked Data

• dbSNP Id: rs1844263272
• gnomAD v4: 10-86668370-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86668374del , CM000672.2:g.86668374del	GRCh38
NC_000010.10:g.88428131del , CM000672.1:g.88428131del	GRCh37
NC_000010.9:g.88418111del	NCBI36
NG_008876.1:g.4811del , LRG_385:g.4811del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443292.2:c.1487-295del	ENSP00000393132.2:n.1487-295del
ENST00000685347.1:n.1449-295del
ENST00000687856.1:c.-23-295del	ENSP00000510221.1:n.-23-295del
ENST00000688001.1:c.-23-295del	ENSP00000508987.1:n.-23-295del
ENST00000688785.1:c.-23-295del	ENSP00000509572.1:n.-23-295del
ENST00000691462.1:c.-23-295del	ENSP00000509930.1:n.-23-295del
ENST00000692941.1:n.2070-295del
XM_011539185.1:c.-23-295del	XP_011537487.1:n.-23-295del
XM_011539189.1:c.-23-295del	XP_011537491.1:n.-23-295del
XM_011539193.1:c.-495-295del	XP_011537495.1:n.-495-295del
XM_011539194.1:c.-495-295del	XP_011537496.1:n.-495-295del
XM_011539185.2:c.-23-295del	XP_011537487.1:n.-23-295del
XM_017015606.1:c.-23-295del	XP_016871095.1:n.-23-295del
XM_017015608.1:c.-23-295del	XP_016871097.1:n.-23-295del
XM_017015609.1:c.-23-295del	XP_016871098.1:n.-23-295del
NM_001368063.1:c.-23-295del	NP_001354992.1:n.-23-295del
NM_001368064.1:c.-23-295del	NP_001354993.1:n.-23-295del
NM_001368068.1:c.-23-295del	NP_001354997.1:n.-23-295del