Canonical Allele Identifier: CA1898291

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 384077
• ClinVar RCV Id: RCV000421462 ; RCV002521667
• dbSNP Id: rs779951735
• ExAC: 2:145156801 T / C
• gnomAD v2: 2-145156801-T-C
• gnomAD v4: 2-144399234-T-C
• MyVariant Identifiers: chr2:g.145156801T>C (hg19) ; chr2:g.144399234T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399234T>C , CM000664.2:g.144399234T>C	GRCh38
NC_000002.11:g.145156801T>C , CM000664.1:g.145156801T>C	GRCh37
NC_000002.10:g.144873271T>C	NCBI36
NG_016431.1:g.126158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1802A>G	ENSP00000508434.1:n.*1802A>G
ENST00000440875.6:c.1176A>G	ENSP00000475553.3:p.Pro392=
ENST00000627532.3:c.1953A>G MANE Select	ENSP00000487174.1:p.Pro651=
ENST00000636026.2:c.1953A>G	ENSP00000490776.1:p.Pro651=
ENST00000636179.1:n.1922A>G
ENST00000636413.1:c.1617A>G	ENSP00000490508.1:p.Pro539=
ENST00000636471.1:c.2028A>G	ENSP00000490317.1:p.Pro676=
ENST00000636732.2:c.*1670A>G	ENSP00000490175.1:n.*1670A>G
ENST00000636820.1:n.2053A>G
ENST00000637045.1:c.1617A>G	ENSP00000490141.1:p.Pro539=
ENST00000637304.1:c.1617A>G	ENSP00000490872.1:p.Pro539=
ENST00000638007.1:c.1617A>G	ENSP00000490723.1:p.Pro539=
ENST00000638087.1:c.1617A>G	ENSP00000490673.1:p.Pro539=
ENST00000638128.1:c.1176A>G	ENSP00000490934.1:p.Pro392=
ENST00000675069.1:c.-133-384A>G	ENSP00000502467.1:n.-133-384A>G
ENST00000675145.1:n.2501A>G
ENST00000303660.8:c.1950A>G	ENSP00000302501.4:p.Pro650=
ENST00000409487.7:c.1953A>G	ENSP00000386854.2:p.Pro651=
ENST00000419938.5:c.655+1965A>G	ENSP00000394777.2:n.655+1965A>G
ENST00000427902.5:c.2040A>G	ENSP00000395496.2:p.Pro680=
ENST00000440875.5:c.1167+303A>G	ENSP00000475553.2:n.1167+303A>G
ENST00000539609.7:c.1881A>G	ENSP00000443792.2:p.Pro627=
ENST00000558170.6:c.1953A>G	ENSP00000454157.1:p.Pro651=
ENST00000627532.2:c.1953A>G	ENSP00000487174.1:p.Pro651=
NM_001171653.1:c.1881A>G	NP_001165124.1:p.Pro627=
NM_014795.3:c.1953A>G	NP_055610.1:p.Pro651=
XM_006712881.2:c.1953A>G	XP_006712944.1:p.Pro651=
XM_006712882.2:c.1953A>G	XP_006712945.1:p.Pro651=
XM_011512231.1:c.1944A>G	XP_011510533.1:p.Pro648=
XM_011512232.1:c.1932A>G	XP_011510534.1:p.Pro644=
NM_014795.4:c.1953A>G MANE Select	NP_055610.1:p.Pro651=
NM_001171653.2:c.1881A>G	NP_001165124.1:p.Pro627=