Canonical Allele Identifier: CA429217592

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1121311
• ClinVar RCV Id: RCV001451536
• dbSNP Id: rs1703230752
• gnomAD v3: 2-144396473-G-A
• gnomAD v4: 2-144396473-G-A
• MyVariant Identifiers: chr2:g.145154040G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396473G>A , CM000664.2:g.144396473G>A	GRCh38
NC_000002.11:g.145154040G>A , CM000664.1:g.145154040G>A	GRCh37
NC_000002.10:g.144870510G>A	NCBI36
NG_016431.1:g.128919C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2855C>T	ENSP00000508434.1:n.*2855C>T
ENST00000440875.6:c.2229C>T	ENSP00000475553.3:p.Asp743=
ENST00000627532.3:c.3006C>T MANE Select	ENSP00000487174.1:p.Asp1002=
ENST00000636026.2:c.3006C>T	ENSP00000490776.1:p.Asp1002=
ENST00000636179.1:n.2975C>T
ENST00000636413.1:c.2670C>T	ENSP00000490508.1:p.Asp890=
ENST00000636471.1:c.3081C>T	ENSP00000490317.1:p.Asp1027=
ENST00000636732.2:c.*2723C>T	ENSP00000490175.1:n.*2723C>T
ENST00000636820.1:n.3106C>T
ENST00000637045.1:c.2670C>T	ENSP00000490141.1:p.Asp890=
ENST00000637304.1:c.2670C>T	ENSP00000490872.1:p.Asp890=
ENST00000638007.1:c.2670C>T	ENSP00000490723.1:p.Asp890=
ENST00000638087.1:c.2670C>T	ENSP00000490673.1:p.Asp890=
ENST00000638128.1:c.2229C>T	ENSP00000490934.1:p.Asp743=
ENST00000639389.1:c.90C>T	ENSP00000492572.1:p.Asp30=
ENST00000647488.1:c.138C>T	ENSP00000494820.1:p.Asp46=
ENST00000675069.1:c.537C>T	ENSP00000502467.1:p.Asp179=
ENST00000303660.8:c.3003C>T	ENSP00000302501.4:p.Asp1001=
ENST00000409487.7:c.3006C>T	ENSP00000386854.2:p.Asp1002=
ENST00000419938.5:c.655+4726C>T	ENSP00000394777.2:n.655+4726C>T
ENST00000539609.7:c.2934C>T	ENSP00000443792.2:p.Asp978=
ENST00000558170.6:c.3006C>T	ENSP00000454157.1:p.Asp1002=
ENST00000627532.2:c.3006C>T	ENSP00000487174.1:p.Asp1002=
NM_001171653.1:c.2934C>T	NP_001165124.1:p.Asp978=
NM_014795.3:c.3006C>T	NP_055610.1:p.Asp1002=
XM_006712881.2:c.3006C>T	XP_006712944.1:p.Asp1002=
XM_006712882.2:c.3006C>T	XP_006712945.1:p.Asp1002=
XM_011512231.1:c.2997C>T	XP_011510533.1:p.Asp999=
XM_011512232.1:c.2985C>T	XP_011510534.1:p.Asp995=
NM_014795.4:c.3006C>T MANE Select	NP_055610.1:p.Asp1002=
NM_001171653.2:c.2934C>T	NP_001165124.1:p.Asp978=