Canonical Allele Identifier: CA790704790

Gene: LDB2

Linked Data

• dbSNP Id: rs1235391912
• gnomAD v3: 4-16892316-C-T
• gnomAD v4: 4-16892316-C-T
• MyVariant Identifiers: chr4:g.16893939C>T (hg19) ; chr4:g.16892316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.16892316C>T , CM000666.2:g.16892316C>T	GRCh38
NC_000004.11:g.16893939C>T , CM000666.1:g.16893939C>T	GRCh37
NC_000004.10:g.16503037C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000304523.10:c.132+6038G>A MANE Select	ENSP00000306772.5:n.132+6038G>A
ENST00000304523.9:c.132+6038G>A	ENSP00000306772.5:n.132+6038G>A
ENST00000441778.6:c.132+6038G>A	ENSP00000392089.2:n.132+6038G>A
ENST00000502640.5:c.132+6038G>A	ENSP00000423963.1:n.132+6038G>A
ENST00000504189.1:n.54+755G>A
ENST00000506732.1:c.60+6038G>A	ENSP00000421767.1:n.60+6038G>A
ENST00000508918.5:c.132+6038G>A	ENSP00000424770.1:n.132+6038G>A
ENST00000510825.5:n.325+6038G>A
ENST00000512345.5:c.132+6038G>A	ENSP00000424676.1:n.132+6038G>A
ENST00000515064.5:c.132+6038G>A	ENSP00000422552.1:n.132+6038G>A
NM_001130834.2:c.132+6038G>A	NP_001124306.1:n.132+6038G>A
NM_001290.4:c.132+6038G>A	NP_001281.1:n.132+6038G>A
NM_001304434.1:c.132+6038G>A	NP_001291363.1:n.132+6038G>A
NM_001304435.1:c.132+6038G>A	NP_001291364.1:n.132+6038G>A
NR_130734.1:n.485+755G>A
XM_005248197.2:c.132+6038G>A	XP_005248254.1:n.132+6038G>A
XM_005248201.2:c.132+6038G>A	XP_005248258.1:n.132+6038G>A
XM_005248202.2:c.132+6038G>A	XP_005248259.1:n.132+6038G>A
XM_006713975.2:c.161+755G>A	XP_006714038.1:n.161+755G>A
XM_006713976.2:c.161+755G>A	XP_006714039.1:n.161+755G>A
XM_006713977.2:c.161+755G>A	XP_006714040.1:n.161+755G>A
XM_006713978.2:c.161+755G>A	XP_006714041.1:n.161+755G>A
XM_006713979.2:c.161+755G>A	XP_006714042.1:n.161+755G>A
XM_006713980.2:c.161+755G>A	XP_006714043.1:n.161+755G>A
XM_006713981.2:c.161+755G>A	XP_006714044.1:n.161+755G>A
XM_006713982.2:c.161+755G>A	XP_006714045.1:n.161+755G>A
XM_006713983.2:c.161+755G>A	XP_006714046.1:n.161+755G>A
XM_011513905.1:c.-146+6038G>A	XP_011512207.1:n.-146+6038G>A
XM_005248197.4:c.132+6038G>A	XP_005248254.1:n.132+6038G>A
XM_005248201.3:c.132+6038G>A	XP_005248258.1:n.132+6038G>A
XM_005248202.3:c.132+6038G>A	XP_005248259.1:n.132+6038G>A
XM_006713975.4:c.161+755G>A	XP_006714038.1:n.161+755G>A
XM_006713976.4:c.161+755G>A	XP_006714039.1:n.161+755G>A
XM_006713977.4:c.161+755G>A	XP_006714040.1:n.161+755G>A
XM_006713978.4:c.161+755G>A	XP_006714041.1:n.161+755G>A
XM_006713979.4:c.161+755G>A	XP_006714042.1:n.161+755G>A
XM_006713980.4:c.161+755G>A	XP_006714043.1:n.161+755G>A
XM_006713981.4:c.161+755G>A	XP_006714044.1:n.161+755G>A
XM_006713982.4:c.161+755G>A	XP_006714045.1:n.161+755G>A
XM_006713983.4:c.161+755G>A	XP_006714046.1:n.161+755G>A
XM_011513905.2:c.-146+6038G>A	XP_011512207.1:n.-146+6038G>A
XM_017008812.2:c.161+755G>A	XP_016864301.1:n.161+755G>A
XM_017008813.2:c.132+6038G>A	XP_016864302.1:n.132+6038G>A
XM_017008814.2:c.161+755G>A	XP_016864303.1:n.161+755G>A
XM_017008815.2:c.161+755G>A	XP_016864304.1:n.161+755G>A
XM_017008816.2:c.161+755G>A	XP_016864305.1:n.161+755G>A
XM_017008817.2:c.132+6038G>A	XP_016864306.1:n.132+6038G>A
XM_017008819.2:c.132+6038G>A	XP_016864308.1:n.132+6038G>A
XM_017008820.2:c.132+6038G>A	XP_016864309.1:n.132+6038G>A
XM_017008821.2:c.132+6038G>A	XP_016864310.1:n.132+6038G>A
XM_017008822.1:c.-325-3558G>A	XP_016864311.1:n.-325-3558G>A
XM_024454278.1:c.132+6038G>A	XP_024310046.1:n.132+6038G>A
XM_024454279.1:c.-425+6038G>A	XP_024310047.1:n.-425+6038G>A
NM_001290.5:c.132+6038G>A MANE Select	NP_001281.1:n.132+6038G>A
NM_001130834.3:c.132+6038G>A	NP_001124306.1:n.132+6038G>A
NM_001304434.2:c.132+6038G>A	NP_001291363.1:n.132+6038G>A
NR_130734.2:n.321+755G>A
NM_001304435.2:c.132+6038G>A	NP_001291364.1:n.132+6038G>A