Canonical Allele Identifier: CA429445156

Gene: ZEB2

Linked Data

• dbSNP Id: rs1703261505
• gnomAD v4: 2-144398547-A-T
• MyVariant Identifiers: chr2:g.145156114A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398547A>T , CM000664.2:g.144398547A>T	GRCh38
NC_000002.11:g.145156114A>T , CM000664.1:g.145156114A>T	GRCh37
NC_000002.10:g.144872584A>T	NCBI36
NG_016431.1:g.126845T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2489T>A	ENSP00000508434.1:n.*2489T>A
ENST00000440875.6:c.1863T>A	ENSP00000475553.3:p.Thr621=
ENST00000627532.3:c.2640T>A MANE Select	ENSP00000487174.1:p.Thr880=
ENST00000636026.2:c.2640T>A	ENSP00000490776.1:p.Thr880=
ENST00000636179.1:n.2609T>A
ENST00000636413.1:c.2304T>A	ENSP00000490508.1:p.Thr768=
ENST00000636471.1:c.2715T>A	ENSP00000490317.1:p.Thr905=
ENST00000636732.2:c.*2357T>A	ENSP00000490175.1:n.*2357T>A
ENST00000636820.1:n.2740T>A
ENST00000637045.1:c.2304T>A	ENSP00000490141.1:p.Thr768=
ENST00000637304.1:c.2304T>A	ENSP00000490872.1:p.Thr768=
ENST00000638007.1:c.2304T>A	ENSP00000490723.1:p.Thr768=
ENST00000638087.1:c.2304T>A	ENSP00000490673.1:p.Thr768=
ENST00000638128.1:c.1863T>A	ENSP00000490934.1:p.Thr621=
ENST00000675069.1:c.171T>A	ENSP00000502467.1:p.Thr57=
ENST00000303660.8:c.2637T>A	ENSP00000302501.4:p.Thr879=
ENST00000409487.7:c.2640T>A	ENSP00000386854.2:p.Thr880=
ENST00000419938.5:c.655+2652T>A	ENSP00000394777.2:n.655+2652T>A
ENST00000440875.5:c.1168-619T>A	ENSP00000475553.2:n.1168-619T>A
ENST00000539609.7:c.2568T>A	ENSP00000443792.2:p.Thr856=
ENST00000558170.6:c.2640T>A	ENSP00000454157.1:p.Thr880=
ENST00000627532.2:c.2640T>A	ENSP00000487174.1:p.Thr880=
NM_001171653.1:c.2568T>A	NP_001165124.1:p.Thr856=
NM_014795.3:c.2640T>A	NP_055610.1:p.Thr880=
XM_006712881.2:c.2640T>A	XP_006712944.1:p.Thr880=
XM_006712882.2:c.2640T>A	XP_006712945.1:p.Thr880=
XM_011512231.1:c.2631T>A	XP_011510533.1:p.Thr877=
XM_011512232.1:c.2619T>A	XP_011510534.1:p.Thr873=
NM_014795.4:c.2640T>A MANE Select	NP_055610.1:p.Thr880=
NM_001171653.2:c.2568T>A	NP_001165124.1:p.Thr856=