Canonical Allele Identifier: CA277036

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 212637
• ClinVar RCV Id: RCV000192869 ; RCV000406872
• dbSNP Id: rs797046122
• MyVariant Identifiers: chr2:g.145161616G>T (hg19) ; chr2:g.144404049G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404049G>T , CM000664.2:g.144404049G>T	GRCh38
NC_000002.11:g.145161616G>T , CM000664.1:g.145161616G>T	GRCh37
NC_000002.10:g.144878086G>T	NCBI36
NG_016431.1:g.121343C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*523C>A	ENSP00000508434.1:n.*523C>A
ENST00000440875.6:c.-104C>A	ENSP00000475553.3:n.-104C>A
ENST00000627532.3:c.674C>A MANE Select	ENSP00000487174.1:p.Ser225Ter
ENST00000636026.2:c.674C>A	ENSP00000490776.1:p.Ser225Ter
ENST00000636179.1:n.643C>A
ENST00000636413.1:c.338C>A	ENSP00000490508.1:p.Ser113Ter
ENST00000636471.1:c.674C>A	ENSP00000490317.1:p.Ser225Ter
ENST00000636732.2:c.*391C>A	ENSP00000490175.1:n.*391C>A
ENST00000636820.1:n.774C>A
ENST00000637045.1:c.338C>A	ENSP00000490141.1:p.Ser113Ter
ENST00000637267.2:c.674C>A	ENSP00000490293.2:p.Ser225Ter
ENST00000637304.1:c.338C>A	ENSP00000490872.1:p.Ser113Ter
ENST00000638007.1:c.338C>A	ENSP00000490723.1:p.Ser113Ter
ENST00000638087.1:c.338C>A	ENSP00000490673.1:p.Ser113Ter
ENST00000638128.1:c.-104C>A	ENSP00000490934.1:n.-104C>A
ENST00000675069.1:c.-133-5199C>A	ENSP00000502467.1:n.-133-5199C>A
ENST00000303660.8:c.671C>A	ENSP00000302501.4:p.Ser224Ter
ENST00000392861.6:c.758C>A	ENSP00000376601.3:p.Ser253Ter
ENST00000409487.7:c.674C>A	ENSP00000386854.2:p.Ser225Ter
ENST00000419938.5:c.413C>A	ENSP00000394777.2:p.Ser138Ter
ENST00000427902.5:c.761C>A	ENSP00000395496.2:p.Ser254Ter
ENST00000440875.5:c.659C>A	ENSP00000475553.2:p.Ser220Ter
ENST00000497268.1:n.620C>A
ENST00000539609.7:c.602C>A	ENSP00000443792.2:p.Ser201Ter
ENST00000558170.6:c.674C>A	ENSP00000454157.1:p.Ser225Ter
ENST00000627532.2:c.674C>A	ENSP00000487174.1:p.Ser225Ter
NM_001171653.1:c.602C>A	NP_001165124.1:p.Ser201Ter
NM_014795.3:c.674C>A	NP_055610.1:p.Ser225Ter
XM_006712881.2:c.674C>A	XP_006712944.1:p.Ser225Ter
XM_006712882.2:c.674C>A	XP_006712945.1:p.Ser225Ter
XM_011512231.1:c.665C>A	XP_011510533.1:p.Ser222Ter
XM_011512232.1:c.653C>A	XP_011510534.1:p.Ser218Ter
NM_014795.4:c.674C>A MANE Select	NP_055610.1:p.Ser225Ter
NM_001171653.2:c.602C>A	NP_001165124.1:p.Ser201Ter