Canonical Allele Identifier: CA57549300

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 703403
• ClinVar RCV Id: RCV001476363
• dbSNP Id: rs907774736
• gnomAD v2: 2-145147168-T-C
• gnomAD v3: 2-144389601-T-C
• gnomAD v4: 2-144389601-T-C
• MyVariant Identifiers: chr2:g.145147168T>C (hg19) ; chr2:g.144389601T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389601T>C , CM000664.2:g.144389601T>C	GRCh38
NC_000002.11:g.145147168T>C , CM000664.1:g.145147168T>C	GRCh37
NC_000002.10:g.144863638T>C	NCBI36
NG_016431.1:g.135791A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3344A>G	ENSP00000508434.1:n.*3344A>G
ENST00000440875.6:c.2718A>G	ENSP00000475553.3:p.Glu906=
ENST00000627532.3:c.3495A>G MANE Select	ENSP00000487174.1:p.Glu1165=
ENST00000636026.2:c.3383A>G	ENSP00000490776.1:p.Lys1128Arg
ENST00000636179.1:n.3464A>G
ENST00000636413.1:c.3159A>G	ENSP00000490508.1:p.Glu1053=
ENST00000636471.1:c.3570A>G	ENSP00000490317.1:p.Glu1190=
ENST00000636732.2:c.*3212A>G	ENSP00000490175.1:n.*3212A>G
ENST00000636820.1:n.3595A>G
ENST00000637045.1:c.3159A>G	ENSP00000490141.1:p.Glu1053=
ENST00000637304.1:c.3159A>G	ENSP00000490872.1:p.Glu1053=
ENST00000638007.1:c.3159A>G	ENSP00000490723.1:p.Glu1053=
ENST00000638087.1:c.3159A>G	ENSP00000490673.1:p.Glu1053=
ENST00000638128.1:c.2718A>G	ENSP00000490934.1:p.Glu906=
ENST00000639389.1:c.151+6811A>G	ENSP00000492572.1:n.151+6811A>G
ENST00000647488.1:c.715A>G	ENSP00000494820.1:n.715A>G
ENST00000675069.1:c.1026A>G	ENSP00000502467.1:p.Glu342=
ENST00000303660.8:c.3492A>G	ENSP00000302501.4:p.Glu1164=
ENST00000409487.7:c.3495A>G	ENSP00000386854.2:p.Glu1165=
ENST00000419938.5:c.656-719A>G	ENSP00000394777.2:n.656-719A>G
ENST00000539609.7:c.3423A>G	ENSP00000443792.2:p.Glu1141=
ENST00000558170.6:c.3495A>G	ENSP00000454157.1:p.Glu1165=
ENST00000627532.2:c.3495A>G	ENSP00000487174.1:p.Glu1165=
NM_001171653.1:c.3423A>G	NP_001165124.1:p.Glu1141=
NM_014795.3:c.3495A>G	NP_055610.1:p.Glu1165=
XM_006712881.2:c.3495A>G	XP_006712944.1:p.Glu1165=
XM_006712882.2:c.3495A>G	XP_006712945.1:p.Glu1165=
XM_011512231.1:c.3486A>G	XP_011510533.1:p.Glu1162=
XM_011512232.1:c.3474A>G	XP_011510534.1:p.Glu1158=
NM_014795.4:c.3495A>G MANE Select	NP_055610.1:p.Glu1165=
NM_001171653.2:c.3423A>G	NP_001165124.1:p.Glu1141=