Canonical Allele Identifier: CA2667209265

Gene: IQCB1

Linked Data

• gnomAD v4: 3-121772447-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121772447A>T , CM000665.2:g.121772447A>T	GRCh38
NC_000003.11:g.121491294A>T , CM000665.1:g.121491294A>T	GRCh37
NC_000003.10:g.122973984A>T	NCBI36
NG_015887.1:g.67633T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310864.11:c.1567+110T>A MANE Select	ENSP00000311505.6:n.1567+110T>A
ENST00000310864.10:c.1567+110T>A	ENSP00000311505.6:n.1567+110T>A
ENST00000349820.10:c.1168+110T>A	ENSP00000323756.7:n.1168+110T>A
ENST00000393650.7:c.*545+110T>A	ENSP00000377261.3:n.*545+110T>A
NM_001023570.2:c.1567+110T>A	NP_001018864.2:n.1567+110T>A
NM_001023571.2:c.1168+110T>A	NP_001018865.2:n.1168+110T>A
XM_005247911.2:c.1411-1873T>A	XP_005247968.1:n.1411-1873T>A
XM_005247912.1:c.1015+110T>A	XP_005247969.1:n.1015+110T>A
XM_011513335.1:c.1015+110T>A	XP_011511637.1:n.1015+110T>A
XR_924221.1:n.1584+110T>A
NM_001023570.3:c.1567+110T>A	NP_001018864.2:n.1567+110T>A
NM_001023571.3:c.1168+110T>A	NP_001018865.2:n.1168+110T>A
NM_001319107.1:c.1567+110T>A	NP_001306036.1:n.1567+110T>A
NR_134968.1:n.1671+110T>A
XM_005247911.4:c.1411-1873T>A	XP_005247968.1:n.1411-1873T>A
XM_005247912.3:c.1015+110T>A	XP_005247969.1:n.1015+110T>A
XM_011513335.3:c.1015+110T>A	XP_011511637.1:n.1015+110T>A
XM_017007537.2:c.1015+110T>A	XP_016863026.1:n.1015+110T>A
XM_017007539.2:c.1012-1873T>A	XP_016863028.1:n.1012-1873T>A
XM_024453833.1:c.1015+110T>A	XP_024309601.1:n.1015+110T>A
XM_024453834.1:c.1015+110T>A	XP_024309602.1:n.1015+110T>A
XR_001740376.2:n.1546+110T>A
XR_001740377.2:n.1390-1873T>A
XR_001740378.2:n.1585+110T>A
XR_001740379.2:n.1436+110T>A
XR_001740380.2:n.1429-1873T>A
XR_001740381.2:n.1280-1873T>A
NM_001023570.4:c.1567+110T>A MANE Select	NP_001018864.2:n.1567+110T>A
NM_001023571.4:c.1168+110T>A	NP_001018865.2:n.1168+110T>A
NM_001319107.2:c.1567+110T>A	NP_001306036.1:n.1567+110T>A
NR_134968.2:n.1652+110T>A