Canonical Allele Identifier: CA57554744

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1145661
• ClinVar RCV Id: RCV001484578 ; RCV002439161
• dbSNP Id: rs780189288
• gnomAD v2: 2-145156012-C-T
• gnomAD v3: 2-144398445-C-T
• gnomAD v4: 2-144398445-C-T
• MyVariant Identifiers: chr2:g.145156012C>T (hg19) ; chr2:g.144398445C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398445C>T , CM000664.2:g.144398445C>T	GRCh38
NC_000002.11:g.145156012C>T , CM000664.1:g.145156012C>T	GRCh37
NC_000002.10:g.144872482C>T	NCBI36
NG_016431.1:g.126947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2591G>A	ENSP00000508434.1:n.*2591G>A
ENST00000440875.6:c.1965G>A	ENSP00000475553.3:p.Gln655=
ENST00000627532.3:c.2742G>A MANE Select	ENSP00000487174.1:p.Gln914=
ENST00000636026.2:c.2742G>A	ENSP00000490776.1:p.Gln914=
ENST00000636179.1:n.2711G>A
ENST00000636413.1:c.2406G>A	ENSP00000490508.1:p.Gln802=
ENST00000636471.1:c.2817G>A	ENSP00000490317.1:p.Gln939=
ENST00000636732.2:c.*2459G>A	ENSP00000490175.1:n.*2459G>A
ENST00000636820.1:n.2842G>A
ENST00000637045.1:c.2406G>A	ENSP00000490141.1:p.Gln802=
ENST00000637304.1:c.2406G>A	ENSP00000490872.1:p.Gln802=
ENST00000638007.1:c.2406G>A	ENSP00000490723.1:p.Gln802=
ENST00000638087.1:c.2406G>A	ENSP00000490673.1:p.Gln802=
ENST00000638128.1:c.1965G>A	ENSP00000490934.1:p.Gln655=
ENST00000675069.1:c.273G>A	ENSP00000502467.1:p.Gln91=
ENST00000303660.8:c.2739G>A	ENSP00000302501.4:p.Gln913=
ENST00000409487.7:c.2742G>A	ENSP00000386854.2:p.Gln914=
ENST00000419938.5:c.655+2754G>A	ENSP00000394777.2:n.655+2754G>A
ENST00000440875.5:c.1168-517G>A	ENSP00000475553.2:n.1168-517G>A
ENST00000539609.7:c.2670G>A	ENSP00000443792.2:p.Gln890=
ENST00000558170.6:c.2742G>A	ENSP00000454157.1:p.Gln914=
ENST00000627532.2:c.2742G>A	ENSP00000487174.1:p.Gln914=
NM_001171653.1:c.2670G>A	NP_001165124.1:p.Gln890=
NM_014795.3:c.2742G>A	NP_055610.1:p.Gln914=
XM_006712881.2:c.2742G>A	XP_006712944.1:p.Gln914=
XM_006712882.2:c.2742G>A	XP_006712945.1:p.Gln914=
XM_011512231.1:c.2733G>A	XP_011510533.1:p.Gln911=
XM_011512232.1:c.2721G>A	XP_011510534.1:p.Gln907=
NM_014795.4:c.2742G>A MANE Select	NP_055610.1:p.Gln914=
NM_001171653.2:c.2670G>A	NP_001165124.1:p.Gln890=