Canonical Allele Identifier: CA348712033

Gene: ZEB2

Linked Data

• dbSNP Id: rs919014269
• gnomAD v3: 2-144399829-A-G
• gnomAD v4: 2-144399829-A-G
• MyVariant Identifiers: chr2:g.145157396A>G (hg19) ; chr2:g.144399829A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399829A>G , CM000664.2:g.144399829A>G	GRCh38
NC_000002.11:g.145157396A>G , CM000664.1:g.145157396A>G	GRCh37
NC_000002.10:g.144873866A>G	NCBI36
NG_016431.1:g.125563T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1207T>C	ENSP00000508434.1:n.*1207T>C
ENST00000440875.6:c.581T>C	ENSP00000475553.3:p.Met194Thr
ENST00000627532.3:c.1358T>C MANE Select	ENSP00000487174.1:p.Met453Thr
ENST00000636026.2:c.1358T>C	ENSP00000490776.1:p.Met453Thr
ENST00000636179.1:n.1327T>C
ENST00000636413.1:c.1022T>C	ENSP00000490508.1:p.Met341Thr
ENST00000636471.1:c.1433T>C	ENSP00000490317.1:p.Met478Thr
ENST00000636732.2:c.*1075T>C	ENSP00000490175.1:n.*1075T>C
ENST00000636820.1:n.1458T>C
ENST00000637045.1:c.1022T>C	ENSP00000490141.1:p.Met341Thr
ENST00000637267.2:c.1358T>C	ENSP00000490293.2:p.Met453Thr
ENST00000637304.1:c.1022T>C	ENSP00000490872.1:p.Met341Thr
ENST00000638007.1:c.1022T>C	ENSP00000490723.1:p.Met341Thr
ENST00000638087.1:c.1022T>C	ENSP00000490673.1:p.Met341Thr
ENST00000638128.1:c.581T>C	ENSP00000490934.1:p.Met194Thr
ENST00000675069.1:c.-133-979T>C	ENSP00000502467.1:n.-133-979T>C
ENST00000675145.1:n.1906T>C
ENST00000303660.8:c.1355T>C	ENSP00000302501.4:p.Met452Thr
ENST00000409487.7:c.1358T>C	ENSP00000386854.2:p.Met453Thr
ENST00000419938.5:c.655+1370T>C	ENSP00000394777.2:n.655+1370T>C
ENST00000427902.5:c.1445T>C	ENSP00000395496.2:p.Met482Thr
ENST00000440875.5:c.1153+190T>C	ENSP00000475553.2:n.1153+190T>C
ENST00000539609.7:c.1286T>C	ENSP00000443792.2:p.Met429Thr
ENST00000558170.6:c.1358T>C	ENSP00000454157.1:p.Met453Thr
ENST00000627532.2:c.1358T>C	ENSP00000487174.1:p.Met453Thr
NM_001171653.1:c.1286T>C	NP_001165124.1:p.Met429Thr
NM_014795.3:c.1358T>C	NP_055610.1:p.Met453Thr
XM_006712881.2:c.1358T>C	XP_006712944.1:p.Met453Thr
XM_006712882.2:c.1358T>C	XP_006712945.1:p.Met453Thr
XM_011512231.1:c.1349T>C	XP_011510533.1:p.Met450Thr
XM_011512232.1:c.1337T>C	XP_011510534.1:p.Met446Thr
NM_014795.4:c.1358T>C MANE Select	NP_055610.1:p.Met453Thr
NM_001171653.2:c.1286T>C	NP_001165124.1:p.Met429Thr