Canonical Allele Identifier: CA348700424

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 837537
• ClinVar RCV Id: RCV001038898
• dbSNP Id: rs1703134304
• MyVariant Identifiers: chr2:g.145147467G>A (hg19) ; chr2:g.144389900G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389900G>A , CM000664.2:g.144389900G>A	GRCh38
NC_000002.11:g.145147467G>A , CM000664.1:g.145147467G>A	GRCh37
NC_000002.10:g.144863937G>A	NCBI36
NG_016431.1:g.135492C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3045C>T	ENSP00000508434.1:n.*3045C>T
ENST00000440875.6:c.2419C>T	ENSP00000475553.3:p.His807Tyr
ENST00000627532.3:c.3196C>T MANE Select	ENSP00000487174.1:p.His1066Tyr
ENST00000636026.2:c.3196C>T	ENSP00000490776.1:p.His1066Tyr
ENST00000636179.1:n.3165C>T
ENST00000636413.1:c.2860C>T	ENSP00000490508.1:p.His954Tyr
ENST00000636471.1:c.3271C>T	ENSP00000490317.1:p.His1091Tyr
ENST00000636732.2:c.*2913C>T	ENSP00000490175.1:n.*2913C>T
ENST00000636820.1:n.3296C>T
ENST00000637045.1:c.2860C>T	ENSP00000490141.1:p.His954Tyr
ENST00000637304.1:c.2860C>T	ENSP00000490872.1:p.His954Tyr
ENST00000638007.1:c.2860C>T	ENSP00000490723.1:p.His954Tyr
ENST00000638087.1:c.2860C>T	ENSP00000490673.1:p.His954Tyr
ENST00000638128.1:c.2419C>T	ENSP00000490934.1:p.His807Tyr
ENST00000639389.1:c.151+6512C>T	ENSP00000492572.1:n.151+6512C>T
ENST00000647488.1:c.416C>T	ENSP00000494820.1:n.416C>T
ENST00000675069.1:c.727C>T	ENSP00000502467.1:p.His243Tyr
ENST00000303660.8:c.3193C>T	ENSP00000302501.4:p.His1065Tyr
ENST00000409487.7:c.3196C>T	ENSP00000386854.2:p.His1066Tyr
ENST00000419938.5:c.656-1018C>T	ENSP00000394777.2:n.656-1018C>T
ENST00000539609.7:c.3124C>T	ENSP00000443792.2:p.His1042Tyr
ENST00000558170.6:c.3196C>T	ENSP00000454157.1:p.His1066Tyr
ENST00000627532.2:c.3196C>T	ENSP00000487174.1:p.His1066Tyr
NM_001171653.1:c.3124C>T	NP_001165124.1:p.His1042Tyr
NM_014795.3:c.3196C>T	NP_055610.1:p.His1066Tyr
XM_006712881.2:c.3196C>T	XP_006712944.1:p.His1066Tyr
XM_006712882.2:c.3196C>T	XP_006712945.1:p.His1066Tyr
XM_011512231.1:c.3187C>T	XP_011510533.1:p.His1063Tyr
XM_011512232.1:c.3175C>T	XP_011510534.1:p.His1059Tyr
NM_014795.4:c.3196C>T MANE Select	NP_055610.1:p.His1066Tyr
NM_001171653.2:c.3124C>T	NP_001165124.1:p.His1042Tyr