Canonical Allele Identifier: CA200804
Gene: IQCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 167197
dbSNP Id: rs727503968

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121790112G>A , CM000665.2:g.121790112G>A GRCh38
NC_000003.11:g.121508959G>A , CM000665.1:g.121508959G>A GRCh37
NC_000003.10:g.122991649G>A NCBI36
NG_015887.1:g.49968C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310864.11:c.1090C>T MANE Select ENSP00000311505.6:p.Arg364Ter
ENST00000310864.10:c.1090C>T ENSP00000311505.6:p.Arg364Ter
ENST00000349820.10:c.691C>T ENSP00000323756.7:p.Arg231Ter
ENST00000393650.7:c.*68C>T ENSP00000377261.3:n.*68C>T
NM_001023570.2:c.1090C>T NP_001018864.2:p.Arg364Ter
NM_001023571.2:c.691C>T NP_001018865.2:p.Arg231Ter
XM_005247911.2:c.1090C>T XP_005247968.1:p.Arg364Ter
XM_005247912.1:c.538C>T XP_005247969.1:p.Arg180Ter
XM_005247913.1:c.1090C>T XP_005247970.1:p.Arg364Ter
XM_011513335.1:c.538C>T XP_011511637.1:p.Arg180Ter
XR_924221.1:n.1107C>T
NM_001023570.3:c.1090C>T NP_001018864.2:p.Arg364Ter
NM_001023571.3:c.691C>T NP_001018865.2:p.Arg231Ter
NM_001319107.1:c.1090C>T NP_001306036.1:p.Arg364Ter
NR_134968.1:n.1194C>T
XM_005247911.4:c.1090C>T XP_005247968.1:p.Arg364Ter
XM_005247912.3:c.538C>T XP_005247969.1:p.Arg180Ter
XM_011513335.3:c.538C>T XP_011511637.1:p.Arg180Ter
XM_017007537.2:c.538C>T XP_016863026.1:p.Arg180Ter
XM_017007539.2:c.691C>T XP_016863028.1:p.Arg231Ter
XM_024453833.1:c.538C>T XP_024309601.1:p.Arg180Ter
XM_024453834.1:c.538C>T XP_024309602.1:p.Arg180Ter
XR_001740376.2:n.1218C>T
XR_001740377.2:n.1218C>T
XR_001740378.2:n.1108C>T
XR_001740379.2:n.1108C>T
XR_001740380.2:n.1108C>T
XR_001740381.2:n.1108C>T
NM_001023570.4:c.1090C>T MANE Select NP_001018864.2:p.Arg364Ter
NM_001023571.4:c.691C>T NP_001018865.2:p.Arg231Ter
NM_001319107.2:c.1090C>T NP_001306036.1:p.Arg364Ter
NR_134968.2:n.1175C>T