Canonical Allele Identifier: CA348710149

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1780413
• ClinVar RCV Id: RCV002410006 ; RCV003611611
• dbSNP Id: rs1703276763
• MyVariant Identifiers: chr2:g.145156953G>A (hg19) ; chr2:g.144399386G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399386G>A , CM000664.2:g.144399386G>A	GRCh38
NC_000002.11:g.145156953G>A , CM000664.1:g.145156953G>A	GRCh37
NC_000002.10:g.144873423G>A	NCBI36
NG_016431.1:g.126006C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1650C>T	ENSP00000508434.1:n.*1650C>T
ENST00000440875.6:c.1024C>T	ENSP00000475553.3:p.Arg342Cys
ENST00000627532.3:c.1801C>T MANE Select	ENSP00000487174.1:p.Arg601Cys
ENST00000636026.2:c.1801C>T	ENSP00000490776.1:p.Arg601Cys
ENST00000636179.1:n.1770C>T
ENST00000636413.1:c.1465C>T	ENSP00000490508.1:p.Arg489Cys
ENST00000636471.1:c.1876C>T	ENSP00000490317.1:p.Arg626Cys
ENST00000636732.2:c.*1518C>T	ENSP00000490175.1:n.*1518C>T
ENST00000636820.1:n.1901C>T
ENST00000637045.1:c.1465C>T	ENSP00000490141.1:p.Arg489Cys
ENST00000637267.2:c.1801C>T	ENSP00000490293.2:p.Arg601Cys
ENST00000637304.1:c.1465C>T	ENSP00000490872.1:p.Arg489Cys
ENST00000638007.1:c.1465C>T	ENSP00000490723.1:p.Arg489Cys
ENST00000638087.1:c.1465C>T	ENSP00000490673.1:p.Arg489Cys
ENST00000638128.1:c.1024C>T	ENSP00000490934.1:p.Arg342Cys
ENST00000675069.1:c.-133-536C>T	ENSP00000502467.1:n.-133-536C>T
ENST00000675145.1:n.2349C>T
ENST00000303660.8:c.1798C>T	ENSP00000302501.4:p.Arg600Cys
ENST00000409487.7:c.1801C>T	ENSP00000386854.2:p.Arg601Cys
ENST00000419938.5:c.655+1813C>T	ENSP00000394777.2:n.655+1813C>T
ENST00000427902.5:c.1888C>T	ENSP00000395496.2:p.Arg630Cys
ENST00000440875.5:c.1167+151C>T	ENSP00000475553.2:n.1167+151C>T
ENST00000539609.7:c.1729C>T	ENSP00000443792.2:p.Arg577Cys
ENST00000558170.6:c.1801C>T	ENSP00000454157.1:p.Arg601Cys
ENST00000627532.2:c.1801C>T	ENSP00000487174.1:p.Arg601Cys
NM_001171653.1:c.1729C>T	NP_001165124.1:p.Arg577Cys
NM_014795.3:c.1801C>T	NP_055610.1:p.Arg601Cys
XM_006712881.2:c.1801C>T	XP_006712944.1:p.Arg601Cys
XM_006712882.2:c.1801C>T	XP_006712945.1:p.Arg601Cys
XM_011512231.1:c.1792C>T	XP_011510533.1:p.Arg598Cys
XM_011512232.1:c.1780C>T	XP_011510534.1:p.Arg594Cys
NM_014795.4:c.1801C>T MANE Select	NP_055610.1:p.Arg601Cys
NM_001171653.2:c.1729C>T	NP_001165124.1:p.Arg577Cys