Canonical Allele Identifier: CA348706636
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1929623
ClinVar RCV Id: RCV002642414
dbSNP Id: rs2149876317

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398341A>G , CM000664.2:g.144398341A>G GRCh38
NC_000002.11:g.145155908A>G , CM000664.1:g.145155908A>G GRCh37
NC_000002.10:g.144872378A>G NCBI36
NG_016431.1:g.127051T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2695T>C ENSP00000508434.1:n.*2695T>C
ENST00000440875.6:c.2069T>C ENSP00000475553.3:p.Met690Thr
ENST00000627532.3:c.2846T>C MANE Select ENSP00000487174.1:p.Met949Thr
ENST00000636026.2:c.2846T>C ENSP00000490776.1:p.Met949Thr
ENST00000636179.1:n.2815T>C
ENST00000636413.1:c.2510T>C ENSP00000490508.1:p.Met837Thr
ENST00000636471.1:c.2921T>C ENSP00000490317.1:p.Met974Thr
ENST00000636732.2:c.*2563T>C ENSP00000490175.1:n.*2563T>C
ENST00000636820.1:n.2946T>C
ENST00000637045.1:c.2510T>C ENSP00000490141.1:p.Met837Thr
ENST00000637304.1:c.2510T>C ENSP00000490872.1:p.Met837Thr
ENST00000638007.1:c.2510T>C ENSP00000490723.1:p.Met837Thr
ENST00000638087.1:c.2510T>C ENSP00000490673.1:p.Met837Thr
ENST00000638128.1:c.2069T>C ENSP00000490934.1:p.Met690Thr
ENST00000675069.1:c.377T>C ENSP00000502467.1:p.Met126Thr
ENST00000303660.8:c.2843T>C ENSP00000302501.4:p.Met948Thr
ENST00000409487.7:c.2846T>C ENSP00000386854.2:p.Met949Thr
ENST00000419938.5:c.655+2858T>C ENSP00000394777.2:n.655+2858T>C
ENST00000440875.5:c.1168-413T>C ENSP00000475553.2:n.1168-413T>C
ENST00000539609.7:c.2774T>C ENSP00000443792.2:p.Met925Thr
ENST00000558170.6:c.2846T>C ENSP00000454157.1:p.Met949Thr
ENST00000627532.2:c.2846T>C ENSP00000487174.1:p.Met949Thr
NM_001171653.1:c.2774T>C NP_001165124.1:p.Met925Thr
NM_014795.3:c.2846T>C NP_055610.1:p.Met949Thr
XM_006712881.2:c.2846T>C XP_006712944.1:p.Met949Thr
XM_006712882.2:c.2846T>C XP_006712945.1:p.Met949Thr
XM_011512231.1:c.2837T>C XP_011510533.1:p.Met946Thr
XM_011512232.1:c.2825T>C XP_011510534.1:p.Met942Thr
NM_014795.4:c.2846T>C MANE Select NP_055610.1:p.Met949Thr
NM_001171653.2:c.2774T>C NP_001165124.1:p.Met925Thr