Canonical Allele Identifier: CA348712009
Gene: ZEB2 HGNC NCBI

Linked Data

dbSNP Id: rs1447536167

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399820T>C , CM000664.2:g.144399820T>C GRCh38
NC_000002.11:g.145157387T>C , CM000664.1:g.145157387T>C GRCh37
NC_000002.10:g.144873857T>C NCBI36
NG_016431.1:g.125572A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1216A>G ENSP00000508434.1:n.*1216A>G
ENST00000440875.6:c.590A>G ENSP00000475553.3:p.Asn197Ser
ENST00000627532.3:c.1367A>G MANE Select ENSP00000487174.1:p.Asn456Ser
ENST00000636026.2:c.1367A>G ENSP00000490776.1:p.Asn456Ser
ENST00000636179.1:n.1336A>G
ENST00000636413.1:c.1031A>G ENSP00000490508.1:p.Asn344Ser
ENST00000636471.1:c.1442A>G ENSP00000490317.1:p.Asn481Ser
ENST00000636732.2:c.*1084A>G ENSP00000490175.1:n.*1084A>G
ENST00000636820.1:n.1467A>G
ENST00000637045.1:c.1031A>G ENSP00000490141.1:p.Asn344Ser
ENST00000637267.2:c.1367A>G ENSP00000490293.2:p.Asn456Ser
ENST00000637304.1:c.1031A>G ENSP00000490872.1:p.Asn344Ser
ENST00000638007.1:c.1031A>G ENSP00000490723.1:p.Asn344Ser
ENST00000638087.1:c.1031A>G ENSP00000490673.1:p.Asn344Ser
ENST00000638128.1:c.590A>G ENSP00000490934.1:p.Asn197Ser
ENST00000675069.1:c.-133-970A>G ENSP00000502467.1:n.-133-970A>G
ENST00000675145.1:n.1915A>G
ENST00000303660.8:c.1364A>G ENSP00000302501.4:p.Asn455Ser
ENST00000409487.7:c.1367A>G ENSP00000386854.2:p.Asn456Ser
ENST00000419938.5:c.655+1379A>G ENSP00000394777.2:n.655+1379A>G
ENST00000427902.5:c.1454A>G ENSP00000395496.2:p.Asn485Ser
ENST00000440875.5:c.1153+199A>G ENSP00000475553.2:n.1153+199A>G
ENST00000539609.7:c.1295A>G ENSP00000443792.2:p.Asn432Ser
ENST00000558170.6:c.1367A>G ENSP00000454157.1:p.Asn456Ser
ENST00000627532.2:c.1367A>G ENSP00000487174.1:p.Asn456Ser
NM_001171653.1:c.1295A>G NP_001165124.1:p.Asn432Ser
NM_014795.3:c.1367A>G NP_055610.1:p.Asn456Ser
XM_006712881.2:c.1367A>G XP_006712944.1:p.Asn456Ser
XM_006712882.2:c.1367A>G XP_006712945.1:p.Asn456Ser
XM_011512231.1:c.1358A>G XP_011510533.1:p.Asn453Ser
XM_011512232.1:c.1346A>G XP_011510534.1:p.Asn449Ser
NM_014795.4:c.1367A>G MANE Select NP_055610.1:p.Asn456Ser
NM_001171653.2:c.1295A>G NP_001165124.1:p.Asn432Ser