Canonical Allele Identifier: CA297599

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 181734
• ClinVar RCV Id: RCV000159474
• dbSNP Id: rs730881195
• ExAC: 2:145157073 T / C
• gnomAD v2: 2-145157073-T-C
• gnomAD v4: 2-144399506-T-C
• MyVariant Identifiers: chr2:g.145157073T>C (hg19) ; chr2:g.144399506T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399506T>C , CM000664.2:g.144399506T>C	GRCh38
NC_000002.11:g.145157073T>C , CM000664.1:g.145157073T>C	GRCh37
NC_000002.10:g.144873543T>C	NCBI36
NG_016431.1:g.125886A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1530A>G	ENSP00000508434.1:n.*1530A>G
ENST00000440875.6:c.904A>G	ENSP00000475553.3:p.Thr302Ala
ENST00000627532.3:c.1681A>G MANE Select	ENSP00000487174.1:p.Thr561Ala
ENST00000636026.2:c.1681A>G	ENSP00000490776.1:p.Thr561Ala
ENST00000636179.1:n.1650A>G
ENST00000636413.1:c.1345A>G	ENSP00000490508.1:p.Thr449Ala
ENST00000636471.1:c.1756A>G	ENSP00000490317.1:p.Thr586Ala
ENST00000636732.2:c.*1398A>G	ENSP00000490175.1:n.*1398A>G
ENST00000636820.1:n.1781A>G
ENST00000637045.1:c.1345A>G	ENSP00000490141.1:p.Thr449Ala
ENST00000637267.2:c.1681A>G	ENSP00000490293.2:p.Thr561Ala
ENST00000637304.1:c.1345A>G	ENSP00000490872.1:p.Thr449Ala
ENST00000638007.1:c.1345A>G	ENSP00000490723.1:p.Thr449Ala
ENST00000638087.1:c.1345A>G	ENSP00000490673.1:p.Thr449Ala
ENST00000638128.1:c.904A>G	ENSP00000490934.1:p.Thr302Ala
ENST00000675069.1:c.-133-656A>G	ENSP00000502467.1:n.-133-656A>G
ENST00000675145.1:n.2229A>G
ENST00000303660.8:c.1678A>G	ENSP00000302501.4:p.Thr560Ala
ENST00000409487.7:c.1681A>G	ENSP00000386854.2:p.Thr561Ala
ENST00000419938.5:c.655+1693A>G	ENSP00000394777.2:n.655+1693A>G
ENST00000427902.5:c.1768A>G	ENSP00000395496.2:p.Thr590Ala
ENST00000440875.5:c.1167+31A>G	ENSP00000475553.2:n.1167+31A>G
ENST00000539609.7:c.1609A>G	ENSP00000443792.2:p.Thr537Ala
ENST00000558170.6:c.1681A>G	ENSP00000454157.1:p.Thr561Ala
ENST00000627532.2:c.1681A>G	ENSP00000487174.1:p.Thr561Ala
NM_001171653.1:c.1609A>G	NP_001165124.1:p.Thr537Ala
NM_014795.3:c.1681A>G	NP_055610.1:p.Thr561Ala
XM_006712881.2:c.1681A>G	XP_006712944.1:p.Thr561Ala
XM_006712882.2:c.1681A>G	XP_006712945.1:p.Thr561Ala
XM_011512231.1:c.1672A>G	XP_011510533.1:p.Thr558Ala
XM_011512232.1:c.1660A>G	XP_011510534.1:p.Thr554Ala
NM_014795.4:c.1681A>G MANE Select	NP_055610.1:p.Thr561Ala
NM_001171653.2:c.1609A>G	NP_001165124.1:p.Thr537Ala