Canonical Allele Identifier: CA348714589

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1369960
• ClinVar RCV Id: RCV001876910
• dbSNP Id: rs2149879143
• MyVariant Identifiers: chr2:g.145161502T>G (hg19) ; chr2:g.144403935T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403935T>G , CM000664.2:g.144403935T>G	GRCh38
NC_000002.11:g.145161502T>G , CM000664.1:g.145161502T>G	GRCh37
NC_000002.10:g.144877972T>G	NCBI36
NG_016431.1:g.121457A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*637A>C	ENSP00000508434.1:n.*637A>C
ENST00000440875.6:c.11A>C	ENSP00000475553.3:p.His4Pro
ENST00000627532.3:c.788A>C MANE Select	ENSP00000487174.1:p.His263Pro
ENST00000636026.2:c.788A>C	ENSP00000490776.1:p.His263Pro
ENST00000636179.1:n.757A>C
ENST00000636413.1:c.452A>C	ENSP00000490508.1:p.His151Pro
ENST00000636471.1:c.788A>C	ENSP00000490317.1:p.His263Pro
ENST00000636732.2:c.*505A>C	ENSP00000490175.1:n.*505A>C
ENST00000636820.1:n.888A>C
ENST00000637045.1:c.452A>C	ENSP00000490141.1:p.His151Pro
ENST00000637267.2:c.788A>C	ENSP00000490293.2:p.His263Pro
ENST00000637304.1:c.452A>C	ENSP00000490872.1:p.His151Pro
ENST00000638007.1:c.452A>C	ENSP00000490723.1:p.His151Pro
ENST00000638087.1:c.452A>C	ENSP00000490673.1:p.His151Pro
ENST00000638128.1:c.11A>C	ENSP00000490934.1:p.His4Pro
ENST00000675069.1:c.-133-5085A>C	ENSP00000502467.1:n.-133-5085A>C
ENST00000303660.8:c.785A>C	ENSP00000302501.4:p.His262Pro
ENST00000392861.6:c.872A>C	ENSP00000376601.3:p.His291Pro
ENST00000409487.7:c.788A>C	ENSP00000386854.2:p.His263Pro
ENST00000419938.5:c.527A>C	ENSP00000394777.2:p.His176Pro
ENST00000427902.5:c.875A>C	ENSP00000395496.2:p.His292Pro
ENST00000440875.5:c.773A>C	ENSP00000475553.2:p.His258Pro
ENST00000539609.7:c.716A>C	ENSP00000443792.2:p.His239Pro
ENST00000558170.6:c.788A>C	ENSP00000454157.1:p.His263Pro
ENST00000627532.2:c.788A>C	ENSP00000487174.1:p.His263Pro
NM_001171653.1:c.716A>C	NP_001165124.1:p.His239Pro
NM_014795.3:c.788A>C	NP_055610.1:p.His263Pro
XM_006712881.2:c.788A>C	XP_006712944.1:p.His263Pro
XM_006712882.2:c.788A>C	XP_006712945.1:p.His263Pro
XM_011512231.1:c.779A>C	XP_011510533.1:p.His260Pro
XM_011512232.1:c.767A>C	XP_011510534.1:p.His256Pro
NM_014795.4:c.788A>C MANE Select	NP_055610.1:p.His263Pro
NM_001171653.2:c.716A>C	NP_001165124.1:p.His239Pro