Canonical Allele Identifier: CA1898226

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 681961
• ClinVar RCV Id: RCV000841938 ; RCV001365027
• dbSNP Id: rs779103467
• ExAC: 2:145156127 T / C
• gnomAD v2: 2-145156127-T-C
• gnomAD v4: 2-144398560-T-C
• MyVariant Identifiers: chr2:g.145156127T>C (hg19) ; chr2:g.144398560T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398560T>C , CM000664.2:g.144398560T>C	GRCh38
NC_000002.11:g.145156127T>C , CM000664.1:g.145156127T>C	GRCh37
NC_000002.10:g.144872597T>C	NCBI36
NG_016431.1:g.126832A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2476A>G	ENSP00000508434.1:n.*2476A>G
ENST00000440875.6:c.1850A>G	ENSP00000475553.3:p.Asp617Gly
ENST00000627532.3:c.2627A>G MANE Select	ENSP00000487174.1:p.Asp876Gly
ENST00000636026.2:c.2627A>G	ENSP00000490776.1:p.Asp876Gly
ENST00000636179.1:n.2596A>G
ENST00000636413.1:c.2291A>G	ENSP00000490508.1:p.Asp764Gly
ENST00000636471.1:c.2702A>G	ENSP00000490317.1:p.Asp901Gly
ENST00000636732.2:c.*2344A>G	ENSP00000490175.1:n.*2344A>G
ENST00000636820.1:n.2727A>G
ENST00000637045.1:c.2291A>G	ENSP00000490141.1:p.Asp764Gly
ENST00000637304.1:c.2291A>G	ENSP00000490872.1:p.Asp764Gly
ENST00000638007.1:c.2291A>G	ENSP00000490723.1:p.Asp764Gly
ENST00000638087.1:c.2291A>G	ENSP00000490673.1:p.Asp764Gly
ENST00000638128.1:c.1850A>G	ENSP00000490934.1:p.Asp617Gly
ENST00000675069.1:c.158A>G	ENSP00000502467.1:p.Asp53Gly
ENST00000303660.8:c.2624A>G	ENSP00000302501.4:p.Asp875Gly
ENST00000409487.7:c.2627A>G	ENSP00000386854.2:p.Asp876Gly
ENST00000419938.5:c.655+2639A>G	ENSP00000394777.2:n.655+2639A>G
ENST00000440875.5:c.1168-632A>G	ENSP00000475553.2:n.1168-632A>G
ENST00000539609.7:c.2555A>G	ENSP00000443792.2:p.Asp852Gly
ENST00000558170.6:c.2627A>G	ENSP00000454157.1:p.Asp876Gly
ENST00000627532.2:c.2627A>G	ENSP00000487174.1:p.Asp876Gly
NM_001171653.1:c.2555A>G	NP_001165124.1:p.Asp852Gly
NM_014795.3:c.2627A>G	NP_055610.1:p.Asp876Gly
XM_006712881.2:c.2627A>G	XP_006712944.1:p.Asp876Gly
XM_006712882.2:c.2627A>G	XP_006712945.1:p.Asp876Gly
XM_011512231.1:c.2618A>G	XP_011510533.1:p.Asp873Gly
XM_011512232.1:c.2606A>G	XP_011510534.1:p.Asp869Gly
NM_014795.4:c.2627A>G MANE Select	NP_055610.1:p.Asp876Gly
NM_001171653.2:c.2555A>G	NP_001165124.1:p.Asp852Gly