Canonical Allele Identifier: CA429445388
Gene: ZEB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.145156903A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399336A>G , CM000664.2:g.144399336A>G GRCh38
NC_000002.11:g.145156903A>G , CM000664.1:g.145156903A>G GRCh37
NC_000002.10:g.144873373A>G NCBI36
NG_016431.1:g.126056T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1700T>C ENSP00000508434.1:n.*1700T>C
ENST00000440875.6:c.1074T>C ENSP00000475553.3:p.His358=
ENST00000627532.3:c.1851T>C MANE Select ENSP00000487174.1:p.His617=
ENST00000636026.2:c.1851T>C ENSP00000490776.1:p.His617=
ENST00000636179.1:n.1820T>C
ENST00000636413.1:c.1515T>C ENSP00000490508.1:p.His505=
ENST00000636471.1:c.1926T>C ENSP00000490317.1:p.His642=
ENST00000636732.2:c.*1568T>C ENSP00000490175.1:n.*1568T>C
ENST00000636820.1:n.1951T>C
ENST00000637045.1:c.1515T>C ENSP00000490141.1:p.His505=
ENST00000637304.1:c.1515T>C ENSP00000490872.1:p.His505=
ENST00000638007.1:c.1515T>C ENSP00000490723.1:p.His505=
ENST00000638087.1:c.1515T>C ENSP00000490673.1:p.His505=
ENST00000638128.1:c.1074T>C ENSP00000490934.1:p.His358=
ENST00000675069.1:c.-133-486T>C ENSP00000502467.1:n.-133-486T>C
ENST00000675145.1:n.2399T>C
ENST00000303660.8:c.1848T>C ENSP00000302501.4:p.His616=
ENST00000409487.7:c.1851T>C ENSP00000386854.2:p.His617=
ENST00000419938.5:c.655+1863T>C ENSP00000394777.2:n.655+1863T>C
ENST00000427902.5:c.1938T>C ENSP00000395496.2:p.His646=
ENST00000440875.5:c.1167+201T>C ENSP00000475553.2:n.1167+201T>C
ENST00000539609.7:c.1779T>C ENSP00000443792.2:p.His593=
ENST00000558170.6:c.1851T>C ENSP00000454157.1:p.His617=
ENST00000627532.2:c.1851T>C ENSP00000487174.1:p.His617=
NM_001171653.1:c.1779T>C NP_001165124.1:p.His593=
NM_014795.3:c.1851T>C NP_055610.1:p.His617=
XM_006712881.2:c.1851T>C XP_006712944.1:p.His617=
XM_006712882.2:c.1851T>C XP_006712945.1:p.His617=
XM_011512231.1:c.1842T>C XP_011510533.1:p.His614=
XM_011512232.1:c.1830T>C XP_011510534.1:p.His610=
NM_014795.4:c.1851T>C MANE Select NP_055610.1:p.His617=
NM_001171653.2:c.1779T>C NP_001165124.1:p.His593=