Canonical Allele Identifier: CA348700233

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147444G>C (hg19) ; chr2:g.144389877G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389877G>C , CM000664.2:g.144389877G>C	GRCh38
NC_000002.11:g.145147444G>C , CM000664.1:g.145147444G>C	GRCh37
NC_000002.10:g.144863914G>C	NCBI36
NG_016431.1:g.135515C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3068C>G	ENSP00000508434.1:n.*3068C>G
ENST00000440875.6:c.2442C>G	ENSP00000475553.3:p.His814Gln
ENST00000627532.3:c.3219C>G MANE Select	ENSP00000487174.1:p.His1073Gln
ENST00000636026.2:c.3219C>G	ENSP00000490776.1:p.His1073Gln
ENST00000636179.1:n.3188C>G
ENST00000636413.1:c.2883C>G	ENSP00000490508.1:p.His961Gln
ENST00000636471.1:c.3294C>G	ENSP00000490317.1:p.His1098Gln
ENST00000636732.2:c.*2936C>G	ENSP00000490175.1:n.*2936C>G
ENST00000636820.1:n.3319C>G
ENST00000637045.1:c.2883C>G	ENSP00000490141.1:p.His961Gln
ENST00000637304.1:c.2883C>G	ENSP00000490872.1:p.His961Gln
ENST00000638007.1:c.2883C>G	ENSP00000490723.1:p.His961Gln
ENST00000638087.1:c.2883C>G	ENSP00000490673.1:p.His961Gln
ENST00000638128.1:c.2442C>G	ENSP00000490934.1:p.His814Gln
ENST00000639389.1:c.151+6535C>G	ENSP00000492572.1:n.151+6535C>G
ENST00000647488.1:c.439C>G	ENSP00000494820.1:n.439C>G
ENST00000675069.1:c.750C>G	ENSP00000502467.1:p.His250Gln
ENST00000303660.8:c.3216C>G	ENSP00000302501.4:p.His1072Gln
ENST00000409487.7:c.3219C>G	ENSP00000386854.2:p.His1073Gln
ENST00000419938.5:c.656-995C>G	ENSP00000394777.2:n.656-995C>G
ENST00000539609.7:c.3147C>G	ENSP00000443792.2:p.His1049Gln
ENST00000558170.6:c.3219C>G	ENSP00000454157.1:p.His1073Gln
ENST00000627532.2:c.3219C>G	ENSP00000487174.1:p.His1073Gln
NM_001171653.1:c.3147C>G	NP_001165124.1:p.His1049Gln
NM_014795.3:c.3219C>G	NP_055610.1:p.His1073Gln
XM_006712881.2:c.3219C>G	XP_006712944.1:p.His1073Gln
XM_006712882.2:c.3219C>G	XP_006712945.1:p.His1073Gln
XM_011512231.1:c.3210C>G	XP_011510533.1:p.His1070Gln
XM_011512232.1:c.3198C>G	XP_011510534.1:p.His1066Gln
NM_014795.4:c.3219C>G MANE Select	NP_055610.1:p.His1073Gln
NM_001171653.2:c.3147C>G	NP_001165124.1:p.His1049Gln