Canonical Allele Identifier: CA348706918

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1309081
• ClinVar RCV Id: RCV001763592
• dbSNP Id: rs2149876375
• MyVariant Identifiers: chr2:g.145155962A>C (hg19) ; chr2:g.144398395A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398395A>C , CM000664.2:g.144398395A>C	GRCh38
NC_000002.11:g.145155962A>C , CM000664.1:g.145155962A>C	GRCh37
NC_000002.10:g.144872432A>C	NCBI36
NG_016431.1:g.126997T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2641T>G	ENSP00000508434.1:n.*2641T>G
ENST00000440875.6:c.2015T>G	ENSP00000475553.3:p.Phe672Cys
ENST00000627532.3:c.2792T>G MANE Select	ENSP00000487174.1:p.Phe931Cys
ENST00000636026.2:c.2792T>G	ENSP00000490776.1:p.Phe931Cys
ENST00000636179.1:n.2761T>G
ENST00000636413.1:c.2456T>G	ENSP00000490508.1:p.Phe819Cys
ENST00000636471.1:c.2867T>G	ENSP00000490317.1:p.Phe956Cys
ENST00000636732.2:c.*2509T>G	ENSP00000490175.1:n.*2509T>G
ENST00000636820.1:n.2892T>G
ENST00000637045.1:c.2456T>G	ENSP00000490141.1:p.Phe819Cys
ENST00000637304.1:c.2456T>G	ENSP00000490872.1:p.Phe819Cys
ENST00000638007.1:c.2456T>G	ENSP00000490723.1:p.Phe819Cys
ENST00000638087.1:c.2456T>G	ENSP00000490673.1:p.Phe819Cys
ENST00000638128.1:c.2015T>G	ENSP00000490934.1:p.Phe672Cys
ENST00000675069.1:c.323T>G	ENSP00000502467.1:p.Phe108Cys
ENST00000303660.8:c.2789T>G	ENSP00000302501.4:p.Phe930Cys
ENST00000409487.7:c.2792T>G	ENSP00000386854.2:p.Phe931Cys
ENST00000419938.5:c.655+2804T>G	ENSP00000394777.2:n.655+2804T>G
ENST00000440875.5:c.1168-467T>G	ENSP00000475553.2:n.1168-467T>G
ENST00000539609.7:c.2720T>G	ENSP00000443792.2:p.Phe907Cys
ENST00000558170.6:c.2792T>G	ENSP00000454157.1:p.Phe931Cys
ENST00000627532.2:c.2792T>G	ENSP00000487174.1:p.Phe931Cys
NM_001171653.1:c.2720T>G	NP_001165124.1:p.Phe907Cys
NM_014795.3:c.2792T>G	NP_055610.1:p.Phe931Cys
XM_006712881.2:c.2792T>G	XP_006712944.1:p.Phe931Cys
XM_006712882.2:c.2792T>G	XP_006712945.1:p.Phe931Cys
XM_011512231.1:c.2783T>G	XP_011510533.1:p.Phe928Cys
XM_011512232.1:c.2771T>G	XP_011510534.1:p.Phe924Cys
NM_014795.4:c.2792T>G MANE Select	NP_055610.1:p.Phe931Cys
NM_001171653.2:c.2720T>G	NP_001165124.1:p.Phe907Cys