Canonical Allele Identifier: CA758235773
Gene: ZEB2 HGNC NCBI

Linked Data

dbSNP Id: rs1360111638

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389385A>G , CM000664.2:g.144389385A>G GRCh38
NC_000002.11:g.145146952A>G , CM000664.1:g.145146952A>G GRCh37
NC_000002.10:g.144863422A>G NCBI36
NG_016431.1:g.136007T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3560T>C ENSP00000508434.1:n.*3560T>C
ENST00000440875.6:c.*66T>C ENSP00000475553.3:n.*66T>C
ENST00000627532.3:c.*66T>C MANE Select ENSP00000487174.1:n.*66T>C
ENST00000636026.2:c.3599T>C ENSP00000490776.1:p.Leu1200Pro
ENST00000636179.1:n.3680T>C
ENST00000636413.1:c.*66T>C ENSP00000490508.1:n.*66T>C
ENST00000636471.1:c.*66T>C ENSP00000490317.1:n.*66T>C
ENST00000636732.2:c.*3428T>C ENSP00000490175.1:n.*3428T>C
ENST00000636820.1:n.3811T>C
ENST00000637045.1:c.*66T>C ENSP00000490141.1:n.*66T>C
ENST00000637304.1:c.*66T>C ENSP00000490872.1:n.*66T>C
ENST00000638007.1:c.*66T>C ENSP00000490723.1:n.*66T>C
ENST00000638087.1:c.*66T>C ENSP00000490673.1:n.*66T>C
ENST00000638128.1:c.*66T>C ENSP00000490934.1:n.*66T>C
ENST00000639389.1:c.151+7027T>C ENSP00000492572.1:n.151+7027T>C
ENST00000647488.1:c.931T>C ENSP00000494820.1:n.931T>C
ENST00000675069.1:c.*66T>C ENSP00000502467.1:n.*66T>C
ENST00000303660.8:c.*66T>C ENSP00000302501.4:n.*66T>C
ENST00000409487.7:c.*66T>C ENSP00000386854.2:n.*66T>C
ENST00000419938.5:c.656-503T>C ENSP00000394777.2:n.656-503T>C
ENST00000539609.7:c.*66T>C ENSP00000443792.2:n.*66T>C
ENST00000558170.6:c.*66T>C ENSP00000454157.1:n.*66T>C
ENST00000627532.2:c.*66T>C ENSP00000487174.1:n.*66T>C
NM_001171653.1:c.*66T>C NP_001165124.1:n.*66T>C
NM_014795.3:c.*66T>C NP_055610.1:n.*66T>C
XM_006712881.2:c.*66T>C XP_006712944.1:n.*66T>C
XM_006712882.2:c.*66T>C XP_006712945.1:n.*66T>C
XM_011512231.1:c.*66T>C XP_011510533.1:n.*66T>C
XM_011512232.1:c.*66T>C XP_011510534.1:n.*66T>C
NM_014795.4:c.*66T>C MANE Select NP_055610.1:n.*66T>C
NM_001171653.2:c.*66T>C NP_001165124.1:n.*66T>C