Canonical Allele Identifier: CA16603872

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 387314
• ClinVar RCV Id: RCV000417838
• dbSNP Id: rs1057522759
• MyVariant Identifiers: chr2:g.145147012A>C (hg19) ; chr2:g.144389445A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389445A>C , CM000664.2:g.144389445A>C	GRCh38
NC_000002.11:g.145147012A>C , CM000664.1:g.145147012A>C	GRCh37
NC_000002.10:g.144863482A>C	NCBI36
NG_016431.1:g.135947T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3500T>G	ENSP00000508434.1:n.*3500T>G
ENST00000440875.6:c.*6T>G	ENSP00000475553.3:n.*6T>G
ENST00000627532.3:c.*6T>G MANE Select	ENSP00000487174.1:n.*6T>G
ENST00000636026.2:c.3539T>G	ENSP00000490776.1:p.Leu1180Arg
ENST00000636179.1:n.3620T>G
ENST00000636413.1:c.*6T>G	ENSP00000490508.1:n.*6T>G
ENST00000636471.1:c.*6T>G	ENSP00000490317.1:n.*6T>G
ENST00000636732.2:c.*3368T>G	ENSP00000490175.1:n.*3368T>G
ENST00000636820.1:n.3751T>G
ENST00000637045.1:c.*6T>G	ENSP00000490141.1:n.*6T>G
ENST00000637304.1:c.*6T>G	ENSP00000490872.1:n.*6T>G
ENST00000638007.1:c.*6T>G	ENSP00000490723.1:n.*6T>G
ENST00000638087.1:c.*6T>G	ENSP00000490673.1:n.*6T>G
ENST00000638128.1:c.*6T>G	ENSP00000490934.1:n.*6T>G
ENST00000639389.1:c.151+6967T>G	ENSP00000492572.1:n.151+6967T>G
ENST00000647488.1:c.871T>G	ENSP00000494820.1:n.871T>G
ENST00000675069.1:c.*6T>G	ENSP00000502467.1:n.*6T>G
ENST00000303660.8:c.*6T>G	ENSP00000302501.4:n.*6T>G
ENST00000409487.7:c.*6T>G	ENSP00000386854.2:n.*6T>G
ENST00000419938.5:c.656-563T>G	ENSP00000394777.2:n.656-563T>G
ENST00000539609.7:c.*6T>G	ENSP00000443792.2:n.*6T>G
ENST00000558170.6:c.*6T>G	ENSP00000454157.1:n.*6T>G
ENST00000627532.2:c.*6T>G	ENSP00000487174.1:n.*6T>G
NM_001171653.1:c.*6T>G	NP_001165124.1:n.*6T>G
NM_014795.3:c.*6T>G	NP_055610.1:n.*6T>G
XM_006712881.2:c.*6T>G	XP_006712944.1:n.*6T>G
XM_006712882.2:c.*6T>G	XP_006712945.1:n.*6T>G
XM_011512231.1:c.*6T>G	XP_011510533.1:n.*6T>G
XM_011512232.1:c.*6T>G	XP_011510534.1:n.*6T>G
NM_014795.4:c.*6T>G MANE Select	NP_055610.1:n.*6T>G
NM_001171653.2:c.*6T>G	NP_001165124.1:n.*6T>G