Canonical Allele Identifier: CA253288
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4768
ClinVar RCV Id: RCV000005034
dbSNP Id: rs137852983

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389740T>C , CM000664.2:g.144389740T>C GRCh38
NC_000002.11:g.145147307T>C , CM000664.1:g.145147307T>C GRCh37
NC_000002.10:g.144863777T>C NCBI36
NG_016431.1:g.135652A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3205A>G ENSP00000508434.1:n.*3205A>G
ENST00000440875.6:c.2579A>G ENSP00000475553.3:p.Gln860Arg
ENST00000627532.3:c.3356A>G MANE Select ENSP00000487174.1:p.Gln1119Arg
ENST00000636026.2:c.3244A>G ENSP00000490776.1:p.Arg1082Gly
ENST00000636179.1:n.3325A>G
ENST00000636413.1:c.3020A>G ENSP00000490508.1:p.Gln1007Arg
ENST00000636471.1:c.3431A>G ENSP00000490317.1:p.Gln1144Arg
ENST00000636732.2:c.*3073A>G ENSP00000490175.1:n.*3073A>G
ENST00000636820.1:n.3456A>G
ENST00000637045.1:c.3020A>G ENSP00000490141.1:p.Gln1007Arg
ENST00000637304.1:c.3020A>G ENSP00000490872.1:p.Gln1007Arg
ENST00000638007.1:c.3020A>G ENSP00000490723.1:p.Gln1007Arg
ENST00000638087.1:c.3020A>G ENSP00000490673.1:p.Gln1007Arg
ENST00000638128.1:c.2579A>G ENSP00000490934.1:p.Gln860Arg
ENST00000639389.1:c.151+6672A>G ENSP00000492572.1:n.151+6672A>G
ENST00000647488.1:c.576A>G ENSP00000494820.1:n.576A>G
ENST00000675069.1:c.887A>G ENSP00000502467.1:p.Gln296Arg
ENST00000303660.8:c.3353A>G ENSP00000302501.4:p.Gln1118Arg
ENST00000409487.7:c.3356A>G ENSP00000386854.2:p.Gln1119Arg
ENST00000419938.5:c.656-858A>G ENSP00000394777.2:n.656-858A>G
ENST00000539609.7:c.3284A>G ENSP00000443792.2:p.Gln1095Arg
ENST00000558170.6:c.3356A>G ENSP00000454157.1:p.Gln1119Arg
ENST00000627532.2:c.3356A>G ENSP00000487174.1:p.Gln1119Arg
NM_001171653.1:c.3284A>G NP_001165124.1:p.Gln1095Arg
NM_014795.3:c.3356A>G NP_055610.1:p.Gln1119Arg
XM_006712881.2:c.3356A>G XP_006712944.1:p.Gln1119Arg
XM_006712882.2:c.3356A>G XP_006712945.1:p.Gln1119Arg
XM_011512231.1:c.3347A>G XP_011510533.1:p.Gln1116Arg
XM_011512232.1:c.3335A>G XP_011510534.1:p.Gln1112Arg
NM_014795.4:c.3356A>G MANE Select NP_055610.1:p.Gln1119Arg
NM_001171653.2:c.3284A>G NP_001165124.1:p.Gln1095Arg