Canonical Allele Identifier: CA2661360198

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2801984
• ClinVar RCV Id: RCV003612505
• gnomAD v4: 2-144403908-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403908C>G , CM000664.2:g.144403908C>G	GRCh38
NC_000002.11:g.145161475C>G , CM000664.1:g.145161475C>G	GRCh37
NC_000002.10:g.144877945C>G	NCBI36
NG_016431.1:g.121484G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*656+8G>C	ENSP00000508434.1:n.*656+8G>C
ENST00000440875.6:c.30+8G>C	ENSP00000475553.3:n.30+8G>C
ENST00000627532.3:c.807+8G>C MANE Select	ENSP00000487174.1:n.807+8G>C
ENST00000636026.2:c.807+8G>C	ENSP00000490776.1:n.807+8G>C
ENST00000636179.1:n.776+8G>C
ENST00000636413.1:c.471+8G>C	ENSP00000490508.1:n.471+8G>C
ENST00000636471.1:c.807+8G>C	ENSP00000490317.1:n.807+8G>C
ENST00000636732.2:c.*524+8G>C	ENSP00000490175.1:n.*524+8G>C
ENST00000636820.1:n.907+8G>C
ENST00000637045.1:c.471+8G>C	ENSP00000490141.1:n.471+8G>C
ENST00000637267.2:c.807+8G>C	ENSP00000490293.2:n.807+8G>C
ENST00000637304.1:c.471+8G>C	ENSP00000490872.1:n.471+8G>C
ENST00000638007.1:c.471+8G>C	ENSP00000490723.1:n.471+8G>C
ENST00000638087.1:c.471+8G>C	ENSP00000490673.1:n.471+8G>C
ENST00000638128.1:c.30+8G>C	ENSP00000490934.1:n.30+8G>C
ENST00000675069.1:c.-133-5058G>C	ENSP00000502467.1:n.-133-5058G>C
ENST00000303660.8:c.804+8G>C	ENSP00000302501.4:n.804+8G>C
ENST00000392861.6:c.891+8G>C	ENSP00000376601.3:n.891+8G>C
ENST00000409487.7:c.807+8G>C	ENSP00000386854.2:n.807+8G>C
ENST00000419938.5:c.546+8G>C	ENSP00000394777.2:n.546+8G>C
ENST00000427902.5:c.894+8G>C	ENSP00000395496.2:n.894+8G>C
ENST00000440875.5:c.792+8G>C	ENSP00000475553.2:n.792+8G>C
ENST00000539609.7:c.735+8G>C	ENSP00000443792.2:n.735+8G>C
ENST00000558170.6:c.807+8G>C	ENSP00000454157.1:n.807+8G>C
ENST00000627532.2:c.807+8G>C	ENSP00000487174.1:n.807+8G>C
NM_001171653.1:c.735+8G>C	NP_001165124.1:n.735+8G>C
NM_014795.3:c.807+8G>C	NP_055610.1:n.807+8G>C
XM_006712881.2:c.807+8G>C	XP_006712944.1:n.807+8G>C
XM_006712882.2:c.807+8G>C	XP_006712945.1:n.807+8G>C
XM_011512231.1:c.798+8G>C	XP_011510533.1:n.798+8G>C
XM_011512232.1:c.786+8G>C	XP_011510534.1:n.786+8G>C
NM_014795.4:c.807+8G>C MANE Select	NP_055610.1:n.807+8G>C
NM_001171653.2:c.735+8G>C	NP_001165124.1:n.735+8G>C