Canonical Allele Identifier: CA1898421

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2781090
• ClinVar RCV Id: RCV003611747
• dbSNP Id: rs771709950
• ExAC: 2:145161528 G / T
• gnomAD v2: 2-145161528-G-T
• gnomAD v4: 2-144403961-G-T
• MyVariant Identifiers: chr2:g.145161528G>T (hg19) ; chr2:g.144403961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403961G>T , CM000664.2:g.144403961G>T	GRCh38
NC_000002.11:g.145161528G>T , CM000664.1:g.145161528G>T	GRCh37
NC_000002.10:g.144877998G>T	NCBI36
NG_016431.1:g.121431C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*611C>A	ENSP00000508434.1:n.*611C>A
ENST00000440875.6:c.-16C>A	ENSP00000475553.3:n.-16C>A
ENST00000627532.3:c.762C>A MANE Select	ENSP00000487174.1:p.Thr254=
ENST00000636026.2:c.762C>A	ENSP00000490776.1:p.Thr254=
ENST00000636179.1:n.731C>A
ENST00000636413.1:c.426C>A	ENSP00000490508.1:p.Thr142=
ENST00000636471.1:c.762C>A	ENSP00000490317.1:p.Thr254=
ENST00000636732.2:c.*479C>A	ENSP00000490175.1:n.*479C>A
ENST00000636820.1:n.862C>A
ENST00000637045.1:c.426C>A	ENSP00000490141.1:p.Thr142=
ENST00000637267.2:c.762C>A	ENSP00000490293.2:p.Thr254=
ENST00000637304.1:c.426C>A	ENSP00000490872.1:p.Thr142=
ENST00000638007.1:c.426C>A	ENSP00000490723.1:p.Thr142=
ENST00000638087.1:c.426C>A	ENSP00000490673.1:p.Thr142=
ENST00000638128.1:c.-16C>A	ENSP00000490934.1:n.-16C>A
ENST00000675069.1:c.-133-5111C>A	ENSP00000502467.1:n.-133-5111C>A
ENST00000303660.8:c.759C>A	ENSP00000302501.4:p.Thr253=
ENST00000392861.6:c.846C>A	ENSP00000376601.3:p.Thr282=
ENST00000409487.7:c.762C>A	ENSP00000386854.2:p.Thr254=
ENST00000419938.5:c.501C>A	ENSP00000394777.2:p.Thr167=
ENST00000427902.5:c.849C>A	ENSP00000395496.2:p.Thr283=
ENST00000440875.5:c.747C>A	ENSP00000475553.2:p.Thr249=
ENST00000539609.7:c.690C>A	ENSP00000443792.2:p.Thr230=
ENST00000558170.6:c.762C>A	ENSP00000454157.1:p.Thr254=
ENST00000627532.2:c.762C>A	ENSP00000487174.1:p.Thr254=
NM_001171653.1:c.690C>A	NP_001165124.1:p.Thr230=
NM_014795.3:c.762C>A	NP_055610.1:p.Thr254=
XM_006712881.2:c.762C>A	XP_006712944.1:p.Thr254=
XM_006712882.2:c.762C>A	XP_006712945.1:p.Thr254=
XM_011512231.1:c.753C>A	XP_011510533.1:p.Thr251=
XM_011512232.1:c.741C>A	XP_011510534.1:p.Thr247=
NM_014795.4:c.762C>A MANE Select	NP_055610.1:p.Thr254=
NM_001171653.2:c.690C>A	NP_001165124.1:p.Thr230=