Canonical Allele Identifier: CA429445493

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1915846
• ClinVar RCV Id: RCV002594133
• dbSNP Id: rs1703266824
• gnomAD v3: 2-144398853-G-C
• gnomAD v4: 2-144398853-G-C
• MyVariant Identifiers: chr2:g.145156420G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398853G>C , CM000664.2:g.144398853G>C	GRCh38
NC_000002.11:g.145156420G>C , CM000664.1:g.145156420G>C	GRCh37
NC_000002.10:g.144872890G>C	NCBI36
NG_016431.1:g.126539C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2183C>G	ENSP00000508434.1:n.*2183C>G
ENST00000440875.6:c.1557C>G	ENSP00000475553.3:p.Ser519=
ENST00000627532.3:c.2334C>G MANE Select	ENSP00000487174.1:p.Ser778=
ENST00000636026.2:c.2334C>G	ENSP00000490776.1:p.Ser778=
ENST00000636179.1:n.2303C>G
ENST00000636413.1:c.1998C>G	ENSP00000490508.1:p.Ser666=
ENST00000636471.1:c.2409C>G	ENSP00000490317.1:p.Ser803=
ENST00000636732.2:c.*2051C>G	ENSP00000490175.1:n.*2051C>G
ENST00000636820.1:n.2434C>G
ENST00000637045.1:c.1998C>G	ENSP00000490141.1:p.Ser666=
ENST00000637304.1:c.1998C>G	ENSP00000490872.1:p.Ser666=
ENST00000638007.1:c.1998C>G	ENSP00000490723.1:p.Ser666=
ENST00000638087.1:c.1998C>G	ENSP00000490673.1:p.Ser666=
ENST00000638128.1:c.1557C>G	ENSP00000490934.1:p.Ser519=
ENST00000675069.1:c.-133-3C>G	ENSP00000502467.1:n.-133-3C>G
ENST00000675145.1:n.2882C>G
ENST00000303660.8:c.2331C>G	ENSP00000302501.4:p.Ser777=
ENST00000409487.7:c.2334C>G	ENSP00000386854.2:p.Ser778=
ENST00000419938.5:c.655+2346C>G	ENSP00000394777.2:n.655+2346C>G
ENST00000440875.5:c.1167+684C>G	ENSP00000475553.2:n.1167+684C>G
ENST00000539609.7:c.2262C>G	ENSP00000443792.2:p.Ser754=
ENST00000558170.6:c.2334C>G	ENSP00000454157.1:p.Ser778=
ENST00000627532.2:c.2334C>G	ENSP00000487174.1:p.Ser778=
NM_001171653.1:c.2262C>G	NP_001165124.1:p.Ser754=
NM_014795.3:c.2334C>G	NP_055610.1:p.Ser778=
XM_006712881.2:c.2334C>G	XP_006712944.1:p.Ser778=
XM_006712882.2:c.2334C>G	XP_006712945.1:p.Ser778=
XM_011512231.1:c.2325C>G	XP_011510533.1:p.Ser775=
XM_011512232.1:c.2313C>G	XP_011510534.1:p.Ser771=
NM_014795.4:c.2334C>G MANE Select	NP_055610.1:p.Ser778=
NM_001171653.2:c.2262C>G	NP_001165124.1:p.Ser754=