Canonical Allele Identifier: CA429445380
Gene: ZEB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.145156333A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398766A>T , CM000664.2:g.144398766A>T GRCh38
NC_000002.11:g.145156333A>T , CM000664.1:g.145156333A>T GRCh37
NC_000002.10:g.144872803A>T NCBI36
NG_016431.1:g.126626T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2270T>A ENSP00000508434.1:n.*2270T>A
ENST00000440875.6:c.1644T>A ENSP00000475553.3:p.Ser548=
ENST00000627532.3:c.2421T>A MANE Select ENSP00000487174.1:p.Ser807=
ENST00000636026.2:c.2421T>A ENSP00000490776.1:p.Ser807=
ENST00000636179.1:n.2390T>A
ENST00000636413.1:c.2085T>A ENSP00000490508.1:p.Ser695=
ENST00000636471.1:c.2496T>A ENSP00000490317.1:p.Ser832=
ENST00000636732.2:c.*2138T>A ENSP00000490175.1:n.*2138T>A
ENST00000636820.1:n.2521T>A
ENST00000637045.1:c.2085T>A ENSP00000490141.1:p.Ser695=
ENST00000637304.1:c.2085T>A ENSP00000490872.1:p.Ser695=
ENST00000638007.1:c.2085T>A ENSP00000490723.1:p.Ser695=
ENST00000638087.1:c.2085T>A ENSP00000490673.1:p.Ser695=
ENST00000638128.1:c.1644T>A ENSP00000490934.1:p.Ser548=
ENST00000675069.1:c.-49T>A ENSP00000502467.1:n.-49T>A
ENST00000675145.1:n.2969T>A
ENST00000303660.8:c.2418T>A ENSP00000302501.4:p.Ser806=
ENST00000409487.7:c.2421T>A ENSP00000386854.2:p.Ser807=
ENST00000419938.5:c.655+2433T>A ENSP00000394777.2:n.655+2433T>A
ENST00000440875.5:c.1167+771T>A ENSP00000475553.2:n.1167+771T>A
ENST00000539609.7:c.2349T>A ENSP00000443792.2:p.Ser783=
ENST00000558170.6:c.2421T>A ENSP00000454157.1:p.Ser807=
ENST00000627532.2:c.2421T>A ENSP00000487174.1:p.Ser807=
NM_001171653.1:c.2349T>A NP_001165124.1:p.Ser783=
NM_014795.3:c.2421T>A NP_055610.1:p.Ser807=
XM_006712881.2:c.2421T>A XP_006712944.1:p.Ser807=
XM_006712882.2:c.2421T>A XP_006712945.1:p.Ser807=
XM_011512231.1:c.2412T>A XP_011510533.1:p.Ser804=
XM_011512232.1:c.2400T>A XP_011510534.1:p.Ser800=
NM_014795.4:c.2421T>A MANE Select NP_055610.1:p.Ser807=
NM_001171653.2:c.2349T>A NP_001165124.1:p.Ser783=