Canonical Allele Identifier: CA273391
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 167860
ClinVar RCV Id: RCV000154160
dbSNP Id: rs727504228

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144429820C>A , CM000664.2:g.144429820C>A GRCh38
NC_000002.11:g.145187387C>A , CM000664.1:g.145187387C>A GRCh37
NC_000002.10:g.144903857C>A NCBI36
NG_016431.1:g.95572G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000637591.2:n.429G>T
ENST00000689298.1:c.*201G>T ENSP00000508434.1:n.*201G>T
ENST00000440875.6:c.-426G>T ENSP00000475553.3:n.-426G>T
ENST00000627532.3:c.280G>T MANE Select ENSP00000487174.1:p.Glu94Ter
ENST00000636026.2:c.280G>T ENSP00000490776.1:p.Glu94Ter
ENST00000636179.1:n.249G>T
ENST00000636413.1:c.-57G>T ENSP00000490508.1:n.-57G>T
ENST00000636471.1:c.280G>T ENSP00000490317.1:p.Glu94Ter
ENST00000636732.2:c.280G>T ENSP00000490175.1:p.Glu94Ter
ENST00000636820.1:n.380G>T
ENST00000637045.1:c.-57G>T ENSP00000490141.1:n.-57G>T
ENST00000637267.2:c.280G>T ENSP00000490293.2:p.Glu94Ter
ENST00000637304.1:c.-57G>T ENSP00000490872.1:n.-57G>T
ENST00000638007.1:c.-57G>T ENSP00000490723.1:n.-57G>T
ENST00000638087.1:c.-57G>T ENSP00000490673.1:n.-57G>T
ENST00000638128.1:c.-426G>T ENSP00000490934.1:n.-426G>T
ENST00000675069.1:c.-133-30970G>T ENSP00000502467.1:n.-133-30970G>T
ENST00000303660.8:c.280G>T ENSP00000302501.4:p.Glu94Ter
ENST00000392861.6:c.364G>T ENSP00000376601.3:p.Glu122Ter
ENST00000409211.5:c.280G>T ENSP00000387256.2:p.Glu94Ter
ENST00000409487.7:c.280G>T ENSP00000386854.2:p.Glu94Ter
ENST00000419938.5:c.280G>T ENSP00000394777.2:p.Glu94Ter
ENST00000427902.5:c.367G>T ENSP00000395496.2:p.Glu123Ter
ENST00000431672.4:c.280G>T ENSP00000475267.2:p.Glu94Ter
ENST00000434448.5:c.*211G>T ENSP00000487261.1:n.*211G>T
ENST00000440875.5:c.265G>T ENSP00000475553.2:p.Glu89Ter
ENST00000461784.3:n.487G>T
ENST00000465308.5:c.280G>T ENSP00000487476.1:p.Glu94Ter
ENST00000472146.5:n.530G>T
ENST00000476394.5:n.384G>T
ENST00000479735.1:n.511G>T
ENST00000539609.7:c.280G>T ENSP00000443792.2:p.Glu94Ter
ENST00000558170.6:c.280G>T ENSP00000454157.1:p.Glu94Ter
ENST00000627532.2:c.280G>T ENSP00000487174.1:p.Glu94Ter
ENST00000627856.2:n.240G>T
NM_001171653.1:c.280G>T NP_001165124.1:p.Glu94Ter
NM_014795.3:c.280G>T NP_055610.1:p.Glu94Ter
XM_006712881.2:c.280G>T XP_006712944.1:p.Glu94Ter
XM_006712882.2:c.280G>T XP_006712945.1:p.Glu94Ter
XM_011512231.1:c.271G>T XP_011510533.1:p.Glu91Ter
XM_011512232.1:c.259G>T XP_011510534.1:p.Glu87Ter
NM_014795.4:c.280G>T MANE Select NP_055610.1:p.Glu94Ter
NM_001171653.2:c.280G>T NP_001165124.1:p.Glu94Ter