Canonical Allele Identifier: CA1898260

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1138433
• ClinVar RCV Id: RCV001474797
• dbSNP Id: rs368984358
• ExAC: 2:145156450 A / G
• gnomAD v2: 2-145156450-A-G
• gnomAD v3: 2-144398883-A-G
• gnomAD v4: 2-144398883-A-G
• MyVariant Identifiers: chr2:g.145156450A>G (hg19) ; chr2:g.144398883A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398883A>G , CM000664.2:g.144398883A>G	GRCh38
NC_000002.11:g.145156450A>G , CM000664.1:g.145156450A>G	GRCh37
NC_000002.10:g.144872920A>G	NCBI36
NG_016431.1:g.126509T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2153T>C	ENSP00000508434.1:n.*2153T>C
ENST00000440875.6:c.1527T>C	ENSP00000475553.3:p.Asn509=
ENST00000627532.3:c.2304T>C MANE Select	ENSP00000487174.1:p.Asn768=
ENST00000636026.2:c.2304T>C	ENSP00000490776.1:p.Asn768=
ENST00000636179.1:n.2273T>C
ENST00000636413.1:c.1968T>C	ENSP00000490508.1:p.Asn656=
ENST00000636471.1:c.2379T>C	ENSP00000490317.1:p.Asn793=
ENST00000636732.2:c.*2021T>C	ENSP00000490175.1:n.*2021T>C
ENST00000636820.1:n.2404T>C
ENST00000637045.1:c.1968T>C	ENSP00000490141.1:p.Asn656=
ENST00000637304.1:c.1968T>C	ENSP00000490872.1:p.Asn656=
ENST00000638007.1:c.1968T>C	ENSP00000490723.1:p.Asn656=
ENST00000638087.1:c.1968T>C	ENSP00000490673.1:p.Asn656=
ENST00000638128.1:c.1527T>C	ENSP00000490934.1:p.Asn509=
ENST00000675069.1:c.-133-33T>C	ENSP00000502467.1:n.-133-33T>C
ENST00000675145.1:n.2852T>C
ENST00000303660.8:c.2301T>C	ENSP00000302501.4:p.Asn767=
ENST00000409487.7:c.2304T>C	ENSP00000386854.2:p.Asn768=
ENST00000419938.5:c.655+2316T>C	ENSP00000394777.2:n.655+2316T>C
ENST00000440875.5:c.1167+654T>C	ENSP00000475553.2:n.1167+654T>C
ENST00000539609.7:c.2232T>C	ENSP00000443792.2:p.Asn744=
ENST00000558170.6:c.2304T>C	ENSP00000454157.1:p.Asn768=
ENST00000627532.2:c.2304T>C	ENSP00000487174.1:p.Asn768=
NM_001171653.1:c.2232T>C	NP_001165124.1:p.Asn744=
NM_014795.3:c.2304T>C	NP_055610.1:p.Asn768=
XM_006712881.2:c.2304T>C	XP_006712944.1:p.Asn768=
XM_006712882.2:c.2304T>C	XP_006712945.1:p.Asn768=
XM_011512231.1:c.2295T>C	XP_011510533.1:p.Asn765=
XM_011512232.1:c.2283T>C	XP_011510534.1:p.Asn761=
NM_014795.4:c.2304T>C MANE Select	NP_055610.1:p.Asn768=
NM_001171653.2:c.2232T>C	NP_001165124.1:p.Asn744=