Canonical Allele Identifier: CA82699947

Gene: IQCB1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121826172C>T , CM000665.2:g.121826172C>T	GRCh38
NC_000003.11:g.121545019C>T , CM000665.1:g.121545019C>T	GRCh37
NC_000003.10:g.123027709C>T	NCBI36
NG_015887.1:g.13908G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310864.11:c.272G>A MANE Select	ENSP00000311505.6:p.Cys91Tyr
ENST00000310864.10:c.272G>A	ENSP00000311505.6:p.Cys91Tyr
ENST00000349820.10:c.272G>A	ENSP00000323756.7:p.Cys91Tyr
ENST00000393650.7:c.272G>A	ENSP00000377261.3:p.Cys91Tyr
ENST00000460108.5:c.-281G>A	ENSP00000419168.1:n.-281G>A
ENST00000498104.1:c.-187G>A	ENSP00000417832.1:n.-187G>A
NM_001023570.2:c.272G>A	NP_001018864.2:p.Cys91Tyr
NM_001023571.2:c.272G>A	NP_001018865.2:p.Cys91Tyr
XM_005247911.2:c.272G>A	XP_005247968.1:p.Cys91Tyr
XM_005247912.1:c.-281G>A	XP_005247969.1:n.-281G>A
XM_005247913.1:c.272G>A	XP_005247970.1:p.Cys91Tyr
XM_011513335.1:c.-187G>A	XP_011511637.1:n.-187G>A
XR_924221.1:n.399G>A
NM_001023570.3:c.272G>A	NP_001018864.2:p.Cys91Tyr
NM_001023571.3:c.272G>A	NP_001018865.2:p.Cys91Tyr
NM_001319107.1:c.272G>A	NP_001306036.1:p.Cys91Tyr
NR_134968.1:n.486G>A
XM_005247911.4:c.272G>A	XP_005247968.1:p.Cys91Tyr
XM_005247912.3:c.-281G>A	XP_005247969.1:n.-281G>A
XM_011513335.3:c.-187G>A	XP_011511637.1:n.-187G>A
XM_017007537.2:c.-187G>A	XP_016863026.1:n.-187G>A
XM_017007539.2:c.272G>A	XP_016863028.1:p.Cys91Tyr
XM_024453833.1:c.-635G>A	XP_024309601.1:n.-635G>A
XM_024453834.1:c.-635G>A	XP_024309602.1:n.-635G>A
XR_001740376.2:n.400G>A
XR_001740377.2:n.400G>A
XR_001740378.2:n.400G>A
XR_001740379.2:n.400G>A
XR_001740380.2:n.400G>A
XR_001740381.2:n.400G>A
NM_001023570.4:c.272G>A MANE Select	NP_001018864.2:p.Cys91Tyr
NM_001023571.4:c.272G>A	NP_001018865.2:p.Cys91Tyr
NM_001319107.2:c.272G>A	NP_001306036.1:p.Cys91Tyr
NR_134968.2:n.467G>A