Canonical Allele Identifier: CA1898249

Gene: ZEB2

Linked Data

• dbSNP Id: rs770951243
• ExAC: 2:145156336 G / A
• gnomAD v2: 2-145156336-G-A
• gnomAD v4: 2-144398769-G-A
• MyVariant Identifiers: chr2:g.145156336G>A (hg19) ; chr2:g.144398769G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398769G>A , CM000664.2:g.144398769G>A	GRCh38
NC_000002.11:g.145156336G>A , CM000664.1:g.145156336G>A	GRCh37
NC_000002.10:g.144872806G>A	NCBI36
NG_016431.1:g.126623C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2267C>T	ENSP00000508434.1:n.*2267C>T
ENST00000440875.6:c.1641C>T	ENSP00000475553.3:p.Phe547=
ENST00000627532.3:c.2418C>T MANE Select	ENSP00000487174.1:p.Phe806=
ENST00000636026.2:c.2418C>T	ENSP00000490776.1:p.Phe806=
ENST00000636179.1:n.2387C>T
ENST00000636413.1:c.2082C>T	ENSP00000490508.1:p.Phe694=
ENST00000636471.1:c.2493C>T	ENSP00000490317.1:p.Phe831=
ENST00000636732.2:c.*2135C>T	ENSP00000490175.1:n.*2135C>T
ENST00000636820.1:n.2518C>T
ENST00000637045.1:c.2082C>T	ENSP00000490141.1:p.Phe694=
ENST00000637304.1:c.2082C>T	ENSP00000490872.1:p.Phe694=
ENST00000638007.1:c.2082C>T	ENSP00000490723.1:p.Phe694=
ENST00000638087.1:c.2082C>T	ENSP00000490673.1:p.Phe694=
ENST00000638128.1:c.1641C>T	ENSP00000490934.1:p.Phe547=
ENST00000675069.1:c.-52C>T	ENSP00000502467.1:n.-52C>T
ENST00000675145.1:n.2966C>T
ENST00000303660.8:c.2415C>T	ENSP00000302501.4:p.Phe805=
ENST00000409487.7:c.2418C>T	ENSP00000386854.2:p.Phe806=
ENST00000419938.5:c.655+2430C>T	ENSP00000394777.2:n.655+2430C>T
ENST00000440875.5:c.1167+768C>T	ENSP00000475553.2:n.1167+768C>T
ENST00000539609.7:c.2346C>T	ENSP00000443792.2:p.Phe782=
ENST00000558170.6:c.2418C>T	ENSP00000454157.1:p.Phe806=
ENST00000627532.2:c.2418C>T	ENSP00000487174.1:p.Phe806=
NM_001171653.1:c.2346C>T	NP_001165124.1:p.Phe782=
NM_014795.3:c.2418C>T	NP_055610.1:p.Phe806=
XM_006712881.2:c.2418C>T	XP_006712944.1:p.Phe806=
XM_006712882.2:c.2418C>T	XP_006712945.1:p.Phe806=
XM_011512231.1:c.2409C>T	XP_011510533.1:p.Phe803=
XM_011512232.1:c.2397C>T	XP_011510534.1:p.Phe799=
NM_014795.4:c.2418C>T MANE Select	NP_055610.1:p.Phe806=
NM_001171653.2:c.2346C>T	NP_001165124.1:p.Phe782=