Canonical Allele Identifier: CA348704892
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144396577C>G , CM000664.2:g.144396577C>G GRCh38
NC_000002.11:g.145154144C>G , CM000664.1:g.145154144C>G GRCh37
NC_000002.10:g.144870614C>G NCBI36
NG_016431.1:g.128815G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*2751G>C ENSP00000508434.1:n.*2751G>C
ENST00000440875.6:c.2125G>C ENSP00000475553.3:p.Gly709Arg
ENST00000627532.3:c.2902G>C MANE Select ENSP00000487174.1:p.Gly968Arg
ENST00000636026.2:c.2902G>C ENSP00000490776.1:p.Gly968Arg
ENST00000636179.1:n.2871G>C
ENST00000636413.1:c.2566G>C ENSP00000490508.1:p.Gly856Arg
ENST00000636471.1:c.2977G>C ENSP00000490317.1:p.Gly993Arg
ENST00000636732.2:c.*2619G>C ENSP00000490175.1:n.*2619G>C
ENST00000636820.1:n.3002G>C
ENST00000637045.1:c.2566G>C ENSP00000490141.1:p.Gly856Arg
ENST00000637304.1:c.2566G>C ENSP00000490872.1:p.Gly856Arg
ENST00000638007.1:c.2566G>C ENSP00000490723.1:p.Gly856Arg
ENST00000638087.1:c.2566G>C ENSP00000490673.1:p.Gly856Arg
ENST00000638128.1:c.2125G>C ENSP00000490934.1:p.Gly709Arg
ENST00000647488.1:c.34G>C ENSP00000494820.1:p.Gly12Arg
ENST00000675069.1:c.433G>C ENSP00000502467.1:p.Gly145Arg
ENST00000303660.8:c.2899G>C ENSP00000302501.4:p.Gly967Arg
ENST00000409487.7:c.2902G>C ENSP00000386854.2:p.Gly968Arg
ENST00000419938.5:c.655+4622G>C ENSP00000394777.2:n.655+4622G>C
ENST00000539609.7:c.2830G>C ENSP00000443792.2:p.Gly944Arg
ENST00000558170.6:c.2902G>C ENSP00000454157.1:p.Gly968Arg
ENST00000627532.2:c.2902G>C ENSP00000487174.1:p.Gly968Arg
NM_001171653.1:c.2830G>C NP_001165124.1:p.Gly944Arg
NM_014795.3:c.2902G>C NP_055610.1:p.Gly968Arg
XM_006712881.2:c.2902G>C XP_006712944.1:p.Gly968Arg
XM_006712882.2:c.2902G>C XP_006712945.1:p.Gly968Arg
XM_011512231.1:c.2893G>C XP_011510533.1:p.Gly965Arg
XM_011512232.1:c.2881G>C XP_011510534.1:p.Gly961Arg
NM_014795.4:c.2902G>C MANE Select NP_055610.1:p.Gly968Arg
NM_001171653.2:c.2830G>C NP_001165124.1:p.Gly944Arg